Canonical Allele Identifier: CA393086534

Gene: HCN4

Linked Data

• gnomAD v4: 15-73323101-G-T
• MyVariant Identifiers: chr15:g.73615442G>T (hg19) ; chr15:g.73323101G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73323101G>T , CM000677.2:g.73323101G>T	GRCh38
NC_000015.9:g.73615442G>T , CM000677.1:g.73615442G>T	GRCh37
NC_000015.8:g.71402495G>T	NCBI36
NG_009063.1:g.51164C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.2992C>A MANE Select	ENSP00000261917.3:p.Pro998Thr
ENST00000261917.3:c.2992C>A	ENSP00000261917.3:p.Pro998Thr
NM_005477.2:c.2992C>A	NP_005468.1:p.Pro998Thr
XM_011521148.1:c.1774C>A	XP_011519450.1:p.Pro592Thr
XM_011521148.2:c.1774C>A	XP_011519450.1:p.Pro592Thr
NM_005477.3:c.2992C>A MANE Select	NP_005468.1:p.Pro998Thr