Canonical Allele Identifier: CA393088372

Gene: HCN4

Linked Data

• dbSNP Id: rs2042876627
• MyVariant Identifiers: chr15:g.73615736C>G (hg19) ; chr15:g.73323395C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73323395C>G , CM000677.2:g.73323395C>G	GRCh38
NC_000015.9:g.73615736C>G , CM000677.1:g.73615736C>G	GRCh37
NC_000015.8:g.71402789C>G	NCBI36
NG_009063.1:g.50870G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000261917.4:c.2698G>C MANE Select	ENSP00000261917.3:p.Ala900Pro
ENST00000261917.3:c.2698G>C	ENSP00000261917.3:p.Ala900Pro
NM_005477.2:c.2698G>C	NP_005468.1:p.Ala900Pro
XM_011521148.1:c.1480G>C	XP_011519450.1:p.Ala494Pro
XM_011521148.2:c.1480G>C	XP_011519450.1:p.Ala494Pro
NM_005477.3:c.2698G>C MANE Select	NP_005468.1:p.Ala900Pro