Canonical Allele Identifier: CA257813559

Gene: MYH7 MIR208B

Linked Data

• dbSNP Id: rs2754157
• MyVariant Identifiers: chr14:g.23887219T>A (hg19) ; chr14:g.23418010T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23418010T>A , CM000676.2:g.23418010T>A	GRCh38
NC_000014.8:g.23887219T>A , CM000676.1:g.23887219T>A	GRCh37
NC_000014.7:g.22957059T>A	NCBI36
NG_007884.1:g.22652A>T , LRG_384:g.22652A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000355349.4:c.4169+200A>T (MYH7) MANE Select	ENSP00000347507.3:n.4169+200A>T
ENST00000355349.3:c.4169+200A>T (MYH7)	ENSP00000347507.3:n.4169+200A>T
NM_000257.3:c.4169+200A>T (MYH7)	NP_000248.2:n.4169+200A>T
NR_030624.1:n.54A>T (MIR208B)
XM_017021340.1:c.4169+200A>T (MYH7)	XP_016876829.1:n.4169+200A>T
NM_000257.4:c.4169+200A>T (MYH7) MANE Select	NP_000248.2:n.4169+200A>T