Canonical Allele Identifier: CA393094043

Gene: HCN4

Linked Data

• MyVariant Identifiers: chr15:g.73622090C>A (hg19) ; chr15:g.73329749C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73329749C>A , CM000677.2:g.73329749C>A	GRCh38
NC_000015.9:g.73622090C>A , CM000677.1:g.73622090C>A	GRCh37
NC_000015.8:g.71409143C>A	NCBI36
NG_009063.1:g.44516G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.1414G>T MANE Select	ENSP00000261917.3:p.Ala472Ser
ENST00000261917.3:c.1414G>T	ENSP00000261917.3:p.Ala472Ser
NM_005477.2:c.1414G>T	NP_005468.1:p.Ala472Ser
XM_011521148.1:c.196G>T	XP_011519450.1:p.Ala66Ser
XM_011521148.2:c.196G>T	XP_011519450.1:p.Ala66Ser
NM_005477.3:c.1414G>T MANE Select	NP_005468.1:p.Ala472Ser