Canonical Allele Identifier: CA7648983

Gene: HCN4

Linked Data

• dbSNP Id: rs749513545
• ExAC: 15:73615793 A / G
• gnomAD v2: 15-73615793-A-G
• gnomAD v4: 15-73323452-A-G
• MyVariant Identifiers: chr15:g.73615793A>G (hg19) ; chr15:g.73323452A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73323452A>G , CM000677.2:g.73323452A>G	GRCh38
NC_000015.9:g.73615793A>G , CM000677.1:g.73615793A>G	GRCh37
NC_000015.8:g.71402846A>G	NCBI36
NG_009063.1:g.50813T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000261917.4:c.2641T>C MANE Select	ENSP00000261917.3:p.Ser881Pro
ENST00000261917.3:c.2641T>C	ENSP00000261917.3:p.Ser881Pro
NM_005477.2:c.2641T>C	NP_005468.1:p.Ser881Pro
XM_011521148.1:c.1423T>C	XP_011519450.1:p.Ser475Pro
XM_011521148.2:c.1423T>C	XP_011519450.1:p.Ser475Pro
NM_005477.3:c.2641T>C MANE Select	NP_005468.1:p.Ser881Pro