Canonical Allele Identifier: CA393089962

Gene: HCN4

Linked Data

• MyVariant Identifiers: chr15:g.73616468G>A (hg19) ; chr15:g.73324127G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73324127G>A , CM000677.2:g.73324127G>A	GRCh38
NC_000015.9:g.73616468G>A , CM000677.1:g.73616468G>A	GRCh37
NC_000015.8:g.71403521G>A	NCBI36
NG_009063.1:g.50138C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261917.4:c.2105C>T MANE Select	ENSP00000261917.3:p.Ala702Val
ENST00000261917.3:c.2105C>T	ENSP00000261917.3:p.Ala702Val
NM_005477.2:c.2105C>T	NP_005468.1:p.Ala702Val
XM_011521148.1:c.887C>T	XP_011519450.1:p.Ala296Val
XM_011521148.2:c.887C>T	XP_011519450.1:p.Ala296Val
NM_005477.3:c.2105C>T MANE Select	NP_005468.1:p.Ala702Val