Canonical Allele Identifier: CA619410713

Gene: HCN4

Linked Data

• dbSNP Id: rs1176575078
• gnomAD v2: 15-73624377-G-A
• gnomAD v3: 15-73332036-G-A
• gnomAD v4: 15-73332036-G-A
• MyVariant Identifiers: chr15:g.73624377G>A (hg19) ; chr15:g.73332036G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73332036G>A , CM000677.2:g.73332036G>A	GRCh38
NC_000015.9:g.73624377G>A , CM000677.1:g.73624377G>A	GRCh37
NC_000015.8:g.71411430G>A	NCBI36
NG_009063.1:g.42229C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261917.4:c.1371+95C>T MANE Select	ENSP00000261917.3:n.1371+95C>T
ENST00000261917.3:c.1371+95C>T	ENSP00000261917.3:n.1371+95C>T
NM_005477.2:c.1371+95C>T	NP_005468.1:n.1371+95C>T
XM_011521148.1:c.153+95C>T	XP_011519450.1:n.153+95C>T
XM_011521148.2:c.153+95C>T	XP_011519450.1:n.153+95C>T
NM_005477.3:c.1371+95C>T MANE Select	NP_005468.1:n.1371+95C>T