Canonical Allele Identifier: CA272665439
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs200773333
gnomAD v3: 15-73324126-G-A
gnomAD v4: 15-73324126-G-A
MyVariant Identifiers: chr15:g.73616467G>A (hg19) chr15:g.73324126G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73324126G>A , CM000677.2:g.73324126G>A GRCh38
NC_000015.9:g.73616467G>A , CM000677.1:g.73616467G>A GRCh37
NC_000015.8:g.71403520G>A NCBI36
NG_009063.1:g.50139C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.2106C>T MANE Select ENSP00000261917.3:p.Ala702=
ENST00000261917.3:c.2106C>T ENSP00000261917.3:p.Ala702=
NM_005477.2:c.2106C>T NP_005468.1:p.Ala702=
XM_011521148.1:c.888C>T XP_011519450.1:p.Ala296=
XM_011521148.2:c.888C>T XP_011519450.1:p.Ala296=
NM_005477.3:c.2106C>T MANE Select NP_005468.1:p.Ala702=
Search 100 bp 5'
Search 100 bp 3'