Canonical Allele Identifier: CA272672110
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs1013342681
gnomAD v3: 15-73329729-G-A
gnomAD v4: 15-73329729-G-A
MyVariant Identifiers: chr15:g.73622070G>A (hg19) chr15:g.73329729G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329729G>A , CM000677.2:g.73329729G>A GRCh38
NC_000015.9:g.73622070G>A , CM000677.1:g.73622070G>A GRCh37
NC_000015.8:g.71409123G>A NCBI36
NG_009063.1:g.44536C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.1434C>T MANE Select ENSP00000261917.3:p.Cys478=
ENST00000261917.3:c.1434C>T ENSP00000261917.3:p.Cys478=
NM_005477.2:c.1434C>T NP_005468.1:p.Cys478=
XM_011521148.1:c.216C>T XP_011519450.1:p.Cys72=
XM_011521148.2:c.216C>T XP_011519450.1:p.Cys72=
NM_005477.3:c.1434C>T MANE Select NP_005468.1:p.Cys478=
Search 100 bp 5'
Search 100 bp 3'