Canonical Allele Identifier: CA491151474

Gene: HCN4

Linked Data

• dbSNP Id: rs1294606432
• MyVariant Identifiers: chr15:g.73621959G>C (hg19) ; chr15:g.73329618G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73329618G>C , CM000677.2:g.73329618G>C	GRCh38
NC_000015.9:g.73621959G>C , CM000677.1:g.73621959G>C	GRCh37
NC_000015.8:g.71409012G>C	NCBI36
NG_009063.1:g.44647C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.1545C>G MANE Select	ENSP00000261917.3:p.Ala515=
ENST00000261917.3:c.1545C>G	ENSP00000261917.3:p.Ala515=
NM_005477.2:c.1545C>G	NP_005468.1:p.Ala515=
XM_011521148.1:c.327C>G	XP_011519450.1:p.Ala109=
XM_011521148.2:c.327C>G	XP_011519450.1:p.Ala109=
NM_005477.3:c.1545C>G MANE Select	NP_005468.1:p.Ala515=