Canonical Allele Identifier: CA272673809

Gene: HCN4

Linked Data

• dbSNP Id: rs948107081
• MyVariant Identifiers: chr15:g.73624406C>A (hg19) ; chr15:g.73332065C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73332065C>A , CM000677.2:g.73332065C>A	GRCh38
NC_000015.9:g.73624406C>A , CM000677.1:g.73624406C>A	GRCh37
NC_000015.8:g.71411459C>A	NCBI36
NG_009063.1:g.42200G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261917.4:c.1371+66G>T MANE Select	ENSP00000261917.3:n.1371+66G>T
ENST00000261917.3:c.1371+66G>T	ENSP00000261917.3:n.1371+66G>T
NM_005477.2:c.1371+66G>T	NP_005468.1:n.1371+66G>T
XM_011521148.1:c.153+66G>T	XP_011519450.1:n.153+66G>T
XM_011521148.2:c.153+66G>T	XP_011519450.1:n.153+66G>T
NM_005477.3:c.1371+66G>T MANE Select	NP_005468.1:n.1371+66G>T