Canonical Allele Identifier: CA393088392

Gene: HCN4

Linked Data

• MyVariant Identifiers: chr15:g.73615742C>A (hg19) ; chr15:g.73323401C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73323401C>A , CM000677.2:g.73323401C>A	GRCh38
NC_000015.9:g.73615742C>A , CM000677.1:g.73615742C>A	GRCh37
NC_000015.8:g.71402795C>A	NCBI36
NG_009063.1:g.50864G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261917.4:c.2692G>T MANE Select	ENSP00000261917.3:p.Gly898Cys
ENST00000261917.3:c.2692G>T	ENSP00000261917.3:p.Gly898Cys
NM_005477.2:c.2692G>T	NP_005468.1:p.Gly898Cys
XM_011521148.1:c.1474G>T	XP_011519450.1:p.Gly492Cys
XM_011521148.2:c.1474G>T	XP_011519450.1:p.Gly492Cys
NM_005477.3:c.2692G>T MANE Select	NP_005468.1:p.Gly898Cys