Canonical Allele Identifier: CA7649339
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 470645
dbSNP Id: rs376218786

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73332260G>A , CM000677.2:g.73332260G>A GRCh38
NC_000015.9:g.73624601G>A , CM000677.1:g.73624601G>A GRCh37
NC_000015.8:g.71411654G>A NCBI36
NG_009063.1:g.42005C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.1242C>T MANE Select ENSP00000261917.3:p.Ala414=
ENST00000261917.3:c.1242C>T ENSP00000261917.3:p.Ala414=
NM_005477.2:c.1242C>T NP_005468.1:p.Ala414=
XM_011521148.1:c.24C>T XP_011519450.1:p.Ala8=
XM_011521148.2:c.24C>T XP_011519450.1:p.Ala8=
NM_005477.3:c.1242C>T MANE Select NP_005468.1:p.Ala414=