Canonical Allele Identifier: CA485766489

Linked Data

MyVariant Identifiers: chr14:g.23885519G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23416310G>C , CM000676.2:g.23416310G>C GRCh38
NC_000014.8:g.23885519G>C , CM000676.1:g.23885519G>C GRCh37
NC_000014.7:g.22955359G>C NCBI36
NG_007884.1:g.24352C>G , LRG_384:g.24352C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4647C>G (MYH7) MANE Select ENSP00000347507.3:p.Ala1549=
ENST00000355349.3:c.4647C>G (MYH7) ENSP00000347507.3:p.Ala1549=
NM_000257.3:c.4647C>G (MYH7) NP_000248.2:p.Ala1549=
NR_126491.1:n.558+13G>C (MHRT)
XM_017021340.1:c.4647C>G (MYH7) XP_016876829.1:p.Ala1549=
NM_000257.4:c.4647C>G (MYH7) MANE Select NP_000248.2:p.Ala1549=