Linked Data
ClinVar Variation Id:
3011646
ClinVar RCV Id:
RCV003872709
dbSNP Id:
rs535525636
ExAC:
14:23885060 G / C
gnomAD v2:
14-23885060-G-C
gnomAD v3:
14-23415851-G-C
gnomAD v4:
14-23415851-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.23415851G>C , CM000676.2:g.23415851G>C | GRCh38 |
| NC_000014.8:g.23885060G>C , CM000676.1:g.23885060G>C | GRCh37 |
| NC_000014.7:g.22954900G>C | NCBI36 |
| NG_007884.1:g.24811C>G , LRG_384:g.24811C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000355349.4:c.4954-19C>G (MYH7) MANE Select | ENSP00000347507.3:n.4954-19C>G | |
| ENST00000355349.3:c.4954-19C>G (MYH7) | ENSP00000347507.3:n.4954-19C>G | |
| NM_000257.3:c.4954-19C>G (MYH7) | NP_000248.2:n.4954-19C>G | |
| NR_126491.1:n.261+22G>C (MHRT) | ||
| XM_017021340.1:c.4954-19C>G (MYH7) | XP_016876829.1:n.4954-19C>G | |
| NM_000257.4:c.4954-19C>G (MYH7) MANE Select | NP_000248.2:n.4954-19C>G |