Canonical Allele Identifier: CA393086148

Gene: HCN4

Linked Data

• gnomAD v4: 15-73322957-A-G
• MyVariant Identifiers: chr15:g.73615298A>G (hg19) ; chr15:g.73322957A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73322957A>G , CM000677.2:g.73322957A>G	GRCh38
NC_000015.9:g.73615298A>G , CM000677.1:g.73615298A>G	GRCh37
NC_000015.8:g.71402351A>G	NCBI36
NG_009063.1:g.51308T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.3136T>C MANE Select	ENSP00000261917.3:p.Ser1046Pro
ENST00000261917.3:c.3136T>C	ENSP00000261917.3:p.Ser1046Pro
NM_005477.2:c.3136T>C	NP_005468.1:p.Ser1046Pro
XM_011521148.1:c.1918T>C	XP_011519450.1:p.Ser640Pro
XM_011521148.2:c.1918T>C	XP_011519450.1:p.Ser640Pro
NM_005477.3:c.3136T>C MANE Select	NP_005468.1:p.Ser1046Pro