Canonical Allele Identifier: CA7648827

Gene: HCN4

Linked Data

• dbSNP Id: rs760100398
• ExAC: 15:73615021 G / A
• gnomAD v2: 15-73615021-G-A
• gnomAD v4: 15-73322680-G-A
• MyVariant Identifiers: chr15:g.73615021G>A (hg19) ; chr15:g.73322680G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73322680G>A , CM000677.2:g.73322680G>A	GRCh38
NC_000015.9:g.73615021G>A , CM000677.1:g.73615021G>A	GRCh37
NC_000015.8:g.71402074G>A	NCBI36
NG_009063.1:g.51585C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261917.4:c.3413C>T MANE Select	ENSP00000261917.3:p.Pro1138Leu
ENST00000261917.3:c.3413C>T	ENSP00000261917.3:p.Pro1138Leu
NM_005477.2:c.3413C>T	NP_005468.1:p.Pro1138Leu
XM_011521148.1:c.2195C>T	XP_011519450.1:p.Pro732Leu
XM_011521148.2:c.2195C>T	XP_011519450.1:p.Pro732Leu
NM_005477.3:c.3413C>T MANE Select	NP_005468.1:p.Pro1138Leu