Canonical Allele Identifier: CA393093296

Gene: HCN4

Linked Data

• MyVariant Identifiers: chr15:g.73621912A>G (hg19) ; chr15:g.73329571A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73329571A>G , CM000677.2:g.73329571A>G	GRCh38
NC_000015.9:g.73621912A>G , CM000677.1:g.73621912A>G	GRCh37
NC_000015.8:g.71408965A>G	NCBI36
NG_009063.1:g.44694T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.1590+2T>C MANE Select	ENSP00000261917.3:n.1590+2T>C
ENST00000261917.3:c.1590+2T>C	ENSP00000261917.3:n.1590+2T>C
NM_005477.2:c.1590+2T>C	NP_005468.1:n.1590+2T>C
XM_011521148.1:c.372+2T>C	XP_011519450.1:n.372+2T>C
XM_011521148.2:c.372+2T>C	XP_011519450.1:n.372+2T>C
NM_005477.3:c.1590+2T>C MANE Select	NP_005468.1:n.1590+2T>C