Canonical Allele Identifier: CA2575504165

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23417398T>C , CM000676.2:g.23417398T>C GRCh38
NC_000014.8:g.23886607T>C , CM000676.1:g.23886607T>C GRCh37
NC_000014.7:g.22956447T>C NCBI36
NG_007884.1:g.23264A>G , LRG_384:g.23264A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4354-80A>G (MYH7) MANE Select ENSP00000347507.3:n.4354-80A>G
ENST00000355349.3:c.4354-80A>G (MYH7) ENSP00000347507.3:n.4354-80A>G
NM_000257.3:c.4354-80A>G (MYH7) NP_000248.2:n.4354-80A>G
NR_126491.1:n.813+25T>C (MHRT)
XM_017021340.1:c.4354-80A>G (MYH7) XP_016876829.1:n.4354-80A>G
NM_000257.4:c.4354-80A>G (MYH7) MANE Select NP_000248.2:n.4354-80A>G