Canonical Allele Identifier: CA393085427

Gene: HCN4

Linked Data

• gnomAD v4: 15-73322705-C-A
• MyVariant Identifiers: chr15:g.73615046C>A (hg19) ; chr15:g.73322705C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73322705C>A , CM000677.2:g.73322705C>A	GRCh38
NC_000015.9:g.73615046C>A , CM000677.1:g.73615046C>A	GRCh37
NC_000015.8:g.71402099C>A	NCBI36
NG_009063.1:g.51560G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.3388G>T MANE Select	ENSP00000261917.3:p.Gly1130Trp
ENST00000261917.3:c.3388G>T	ENSP00000261917.3:p.Gly1130Trp
NM_005477.2:c.3388G>T	NP_005468.1:p.Gly1130Trp
XM_011521148.1:c.2170G>T	XP_011519450.1:p.Gly724Trp
XM_011521148.2:c.2170G>T	XP_011519450.1:p.Gly724Trp
NM_005477.3:c.3388G>T MANE Select	NP_005468.1:p.Gly1130Trp