Canonical Allele Identifier: CA2624251938
Gene: MYH6 HGNC NCBI

Linked Data

gnomAD v4: 14-23393612-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23393612T>C , CM000676.2:g.23393612T>C GRCh38
NC_000014.8:g.23862821T>C , CM000676.1:g.23862821T>C GRCh37
NC_000014.7:g.22932661T>C NCBI36
NG_023444.1:g.19666A>G , LRG_389:g.19666A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000405093.9:c.2928+54A>G MANE Select ENSP00000386041.3:n.2928+54A>G
ENST00000356287.3:c.2928+54A>G ENSP00000348634.3:n.2928+54A>G
ENST00000405093.7:c.2928+54A>G ENSP00000386041.3:n.2928+54A>G
NM_002471.3:c.2928+54A>G , LRG_389t1:c.2928+54A>G NP_002462.2:n.2928+54A>G
NM_002471.4:c.2928+54A>G MANE Select NP_002462.2:n.2928+54A>G
Search 100 bp 5'
Search 100 bp 3'