Canonical Allele Identifier: CA491477929
Gene: HCN4 HGNC NCBI

Linked Data

gnomAD v4: 15-73322892-C-T
MyVariant Identifiers: chr15:g.73615233C>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322892C>T , CM000677.2:g.73322892C>T GRCh38
NC_000015.9:g.73615233C>T , CM000677.1:g.73615233C>T GRCh37
NC_000015.8:g.71402286C>T NCBI36
NG_009063.1:g.51373G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.3201G>A MANE Select ENSP00000261917.3:p.Gln1067=
ENST00000261917.3:c.3201G>A ENSP00000261917.3:p.Gln1067=
NM_005477.2:c.3201G>A NP_005468.1:p.Gln1067=
XM_011521148.1:c.1983G>A XP_011519450.1:p.Gln661=
XM_011521148.2:c.1983G>A XP_011519450.1:p.Gln661=
NM_005477.3:c.3201G>A MANE Select NP_005468.1:p.Gln1067=
Search 100 bp 5'
Search 100 bp 3'