Canonical Allele Identifier: CA389050813
Gene: MYH7 HGNC NCBI

Linked Data

dbSNP Id: rs1352198296
MyVariant Identifiers: chr14:g.23898222T>G (hg19) chr14:g.23429013T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23429013T>G , CM000676.2:g.23429013T>G GRCh38
NC_000014.8:g.23898222T>G , CM000676.1:g.23898222T>G GRCh37
NC_000014.7:g.22968062T>G NCBI36
NG_007884.1:g.11649A>C , LRG_384:g.11649A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.1349A>C MANE Select ENSP00000347507.3:p.Lys450Thr
ENST00000355349.3:c.1349A>C ENSP00000347507.3:p.Lys450Thr
NM_000257.3:c.1349A>C NP_000248.2:p.Lys450Thr
XR_245686.3:n.1455A>C
XM_017021340.1:c.1349A>C XP_016876829.1:p.Lys450Thr
NM_000257.4:c.1349A>C MANE Select NP_000248.2:p.Lys450Thr
Search 100 bp 5'
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