Canonical Allele Identifier: CA272673802

Gene: HCN4

Linked Data

• dbSNP Id: rs1055690979
• MyVariant Identifiers: chr15:g.73624376T>C (hg19) ; chr15:g.73332035T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73332035T>C , CM000677.2:g.73332035T>C	GRCh38
NC_000015.9:g.73624376T>C , CM000677.1:g.73624376T>C	GRCh37
NC_000015.8:g.71411429T>C	NCBI36
NG_009063.1:g.42230A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000261917.4:c.1371+96A>G MANE Select	ENSP00000261917.3:n.1371+96A>G
ENST00000261917.3:c.1371+96A>G	ENSP00000261917.3:n.1371+96A>G
NM_005477.2:c.1371+96A>G	NP_005468.1:n.1371+96A>G
XM_011521148.1:c.153+96A>G	XP_011519450.1:n.153+96A>G
XM_011521148.2:c.153+96A>G	XP_011519450.1:n.153+96A>G
NM_005477.3:c.1371+96A>G MANE Select	NP_005468.1:n.1371+96A>G