Canonical Allele Identifier: CA393085018

Gene: HCN4

Linked Data

• MyVariant Identifiers: chr15:g.73614913G>A (hg19) ; chr15:g.73322572G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73322572G>A , CM000677.2:g.73322572G>A	GRCh38
NC_000015.9:g.73614913G>A , CM000677.1:g.73614913G>A	GRCh37
NC_000015.8:g.71401966G>A	NCBI36
NG_009063.1:g.51693C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.3521C>T MANE Select	ENSP00000261917.3:p.Ser1174Phe
ENST00000261917.3:c.3521C>T	ENSP00000261917.3:p.Ser1174Phe
NM_005477.2:c.3521C>T	NP_005468.1:p.Ser1174Phe
XM_011521148.1:c.2303C>T	XP_011519450.1:p.Ser768Phe
XM_011521148.2:c.2303C>T	XP_011519450.1:p.Ser768Phe
NM_005477.3:c.3521C>T MANE Select	NP_005468.1:p.Ser1174Phe