Canonical Allele Identifier: CA491478529

Gene: HCN4

Linked Data

• gnomAD v4: 15-73323711-G-A
• MyVariant Identifiers: chr15:g.73616052G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73323711G>A , CM000677.2:g.73323711G>A	GRCh38
NC_000015.9:g.73616052G>A , CM000677.1:g.73616052G>A	GRCh37
NC_000015.8:g.71403105G>A	NCBI36
NG_009063.1:g.50554C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261917.4:c.2382C>T MANE Select	ENSP00000261917.3:p.Ala794=
ENST00000261917.3:c.2382C>T	ENSP00000261917.3:p.Ala794=
NM_005477.2:c.2382C>T	NP_005468.1:p.Ala794=
XM_011521148.1:c.1164C>T	XP_011519450.1:p.Ala388=
XM_011521148.2:c.1164C>T	XP_011519450.1:p.Ala388=
NM_005477.3:c.2382C>T MANE Select	NP_005468.1:p.Ala794=