Canonical Allele Identifier: CA485766359

Linked Data

MyVariant Identifiers: chr14:g.23885036G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23415827G>T , CM000676.2:g.23415827G>T GRCh38
NC_000014.8:g.23885036G>T , CM000676.1:g.23885036G>T GRCh37
NC_000014.7:g.22954876G>T NCBI36
NG_007884.1:g.24835C>A , LRG_384:g.24835C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4959C>A (MYH7) MANE Select ENSP00000347507.3:p.Thr1653=
ENST00000355349.3:c.4959C>A (MYH7) ENSP00000347507.3:p.Thr1653=
NM_000257.3:c.4959C>A (MYH7) NP_000248.2:p.Thr1653=
NR_126491.1:n.259G>T (MHRT)
XM_017021340.1:c.4959C>A (MYH7) XP_016876829.1:p.Thr1653=
NM_000257.4:c.4959C>A (MYH7) MANE Select NP_000248.2:p.Thr1653=