Canonical Allele Identifier: CA2187185949

Gene: HCN4

Linked Data

• dbSNP Id: rs2042865055
• gnomAD v4: 15-73322444-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73322444G>A , CM000677.2:g.73322444G>A	GRCh38
NC_000015.9:g.73614785G>A , CM000677.1:g.73614785G>A	GRCh37
NC_000015.8:g.71401838G>A	NCBI36
NG_009063.1:g.51821C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.*37C>T MANE Select	ENSP00000261917.3:n.*37C>T
ENST00000261917.3:c.*37C>T	ENSP00000261917.3:n.*37C>T
NM_005477.2:c.*37C>T	NP_005468.1:n.*37C>T
XM_011521148.1:c.*37C>T	XP_011519450.1:n.*37C>T
XM_011521148.2:c.*37C>T	XP_011519450.1:n.*37C>T
NM_005477.3:c.*37C>T MANE Select	NP_005468.1:n.*37C>T