Canonical Allele Identifier: CA272672130

Gene: HCN4

Linked Data

• dbSNP Id: rs1025033466
• MyVariant Identifiers: chr15:g.73622092T>G (hg19) ; chr15:g.73329751T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73329751T>G , CM000677.2:g.73329751T>G	GRCh38
NC_000015.9:g.73622092T>G , CM000677.1:g.73622092T>G	GRCh37
NC_000015.8:g.71409145T>G	NCBI36
NG_009063.1:g.44514A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.1412A>C MANE Select	ENSP00000261917.3:p.Lys471Thr
ENST00000261917.3:c.1412A>C	ENSP00000261917.3:p.Lys471Thr
NM_005477.2:c.1412A>C	NP_005468.1:p.Lys471Thr
XM_011521148.1:c.194A>C	XP_011519450.1:p.Lys65Thr
XM_011521148.2:c.194A>C	XP_011519450.1:p.Lys65Thr
NM_005477.3:c.1412A>C MANE Select	NP_005468.1:p.Lys471Thr