Canonical Allele Identifier: CA2624251963
Gene: MYH6 HGNC NCBI

Linked Data

gnomAD v4: 14-23393631-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23393631A>G , CM000676.2:g.23393631A>G GRCh38
NC_000014.8:g.23862840A>G , CM000676.1:g.23862840A>G GRCh37
NC_000014.7:g.22932680A>G NCBI36
NG_023444.1:g.19647T>C , LRG_389:g.19647T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000405093.9:c.2928+35T>C MANE Select ENSP00000386041.3:n.2928+35T>C
ENST00000356287.3:c.2928+35T>C ENSP00000348634.3:n.2928+35T>C
ENST00000405093.7:c.2928+35T>C ENSP00000386041.3:n.2928+35T>C
NM_002471.3:c.2928+35T>C , LRG_389t1:c.2928+35T>C NP_002462.2:n.2928+35T>C
NM_002471.4:c.2928+35T>C MANE Select NP_002462.2:n.2928+35T>C
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