Canonical Allele Identifier: CA7649268

Gene: HCN4

Linked Data

• dbSNP Id: rs774453547
• ExAC: 15:73621869 C / T
• gnomAD v2: 15-73621869-C-T
• gnomAD v4: 15-73329528-C-T
• MyVariant Identifiers: chr15:g.73621869C>T (hg19) ; chr15:g.73329528C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73329528C>T , CM000677.2:g.73329528C>T	GRCh38
NC_000015.9:g.73621869C>T , CM000677.1:g.73621869C>T	GRCh37
NC_000015.8:g.71408922C>T	NCBI36
NG_009063.1:g.44737G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.1590+45G>A MANE Select	ENSP00000261917.3:n.1590+45G>A
ENST00000261917.3:c.1590+45G>A	ENSP00000261917.3:n.1590+45G>A
NM_005477.2:c.1590+45G>A	NP_005468.1:n.1590+45G>A
XM_011521148.1:c.372+45G>A	XP_011519450.1:n.372+45G>A
XM_011521148.2:c.372+45G>A	XP_011519450.1:n.372+45G>A
NM_005477.3:c.1590+45G>A MANE Select	NP_005468.1:n.1590+45G>A