Canonical Allele Identifier: CA393085358

Gene: HCN4

Linked Data

• gnomAD v4: 15-73322669-A-G
• MyVariant Identifiers: chr15:g.73615010A>G (hg19) ; chr15:g.73322669A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73322669A>G , CM000677.2:g.73322669A>G	GRCh38
NC_000015.9:g.73615010A>G , CM000677.1:g.73615010A>G	GRCh37
NC_000015.8:g.71402063A>G	NCBI36
NG_009063.1:g.51596T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.3424T>C MANE Select	ENSP00000261917.3:p.Tyr1142His
ENST00000261917.3:c.3424T>C	ENSP00000261917.3:p.Tyr1142His
NM_005477.2:c.3424T>C	NP_005468.1:p.Tyr1142His
XM_011521148.1:c.2206T>C	XP_011519450.1:p.Tyr736His
XM_011521148.2:c.2206T>C	XP_011519450.1:p.Tyr736His
NM_005477.3:c.3424T>C MANE Select	NP_005468.1:p.Tyr1142His