Canonical Allele Identifier: CA393097720

Gene: HCN4

Linked Data

• MyVariant Identifiers: chr15:g.73660077A>G (hg19) ; chr15:g.73367736A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73367736A>G , CM000677.2:g.73367736A>G	GRCh38
NC_000015.9:g.73660077A>G , CM000677.1:g.73660077A>G	GRCh37
NC_000015.8:g.71447130A>G	NCBI36
NG_009063.1:g.6529T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.535T>C MANE Select	ENSP00000261917.3:p.Cys179Arg
ENST00000261917.3:c.535T>C	ENSP00000261917.3:p.Cys179Arg
NM_005477.2:c.535T>C	NP_005468.1:p.Cys179Arg
NM_005477.3:c.535T>C MANE Select	NP_005468.1:p.Cys179Arg