Canonical Allele Identifier: CA491478544
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs1333164922
gnomAD v2: 15-73616058-G-A
gnomAD v4: 15-73323717-G-A
MyVariant Identifiers: chr15:g.73616058G>A (hg19) chr15:g.73323717G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323717G>A , CM000677.2:g.73323717G>A GRCh38
NC_000015.9:g.73616058G>A , CM000677.1:g.73616058G>A GRCh37
NC_000015.8:g.71403111G>A NCBI36
NG_009063.1:g.50548C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.2376C>T MANE Select ENSP00000261917.3:p.Ala792=
ENST00000261917.3:c.2376C>T ENSP00000261917.3:p.Ala792=
NM_005477.2:c.2376C>T NP_005468.1:p.Ala792=
XM_011521148.1:c.1158C>T XP_011519450.1:p.Ala386=
XM_011521148.2:c.1158C>T XP_011519450.1:p.Ala386=
NM_005477.3:c.2376C>T MANE Select NP_005468.1:p.Ala792=
Search 100 bp 5'
Search 100 bp 3'