Canonical Allele Identifier: CA393086370

Gene: HCN4

Linked Data

• dbSNP Id: rs2151214164
• MyVariant Identifiers: chr15:g.73615396C>G (hg19) ; chr15:g.73323055C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73323055C>G , CM000677.2:g.73323055C>G	GRCh38
NC_000015.9:g.73615396C>G , CM000677.1:g.73615396C>G	GRCh37
NC_000015.8:g.71402449C>G	NCBI36
NG_009063.1:g.51210G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.3038G>C MANE Select	ENSP00000261917.3:p.Gly1013Ala
ENST00000261917.3:c.3038G>C	ENSP00000261917.3:p.Gly1013Ala
NM_005477.2:c.3038G>C	NP_005468.1:p.Gly1013Ala
XM_011521148.1:c.1820G>C	XP_011519450.1:p.Gly607Ala
XM_011521148.2:c.1820G>C	XP_011519450.1:p.Gly607Ala
NM_005477.3:c.3038G>C MANE Select	NP_005468.1:p.Gly1013Ala