Canonical Allele Identifier: CA491478402
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs1407946956
gnomAD v2: 15-73615395-C-T
MyVariant Identifiers: chr15:g.73615395C>T (hg19) chr15:g.73323054C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323054C>T , CM000677.2:g.73323054C>T GRCh38
NC_000015.9:g.73615395C>T , CM000677.1:g.73615395C>T GRCh37
NC_000015.8:g.71402448C>T NCBI36
NG_009063.1:g.51211G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3039G>A MANE Select ENSP00000261917.3:p.Gly1013=
ENST00000261917.3:c.3039G>A ENSP00000261917.3:p.Gly1013=
NM_005477.2:c.3039G>A NP_005468.1:p.Gly1013=
XM_011521148.1:c.1821G>A XP_011519450.1:p.Gly607=
XM_011521148.2:c.1821G>A XP_011519450.1:p.Gly607=
NM_005477.3:c.3039G>A MANE Select NP_005468.1:p.Gly1013=
Search 100 bp 5'
Search 100 bp 3'