Canonical Allele Identifier: CA491478662
Gene: HCN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.73615791G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323450G>T , CM000677.2:g.73323450G>T GRCh38
NC_000015.9:g.73615791G>T , CM000677.1:g.73615791G>T GRCh37
NC_000015.8:g.71402844G>T NCBI36
NG_009063.1:g.50815C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.2643C>A MANE Select ENSP00000261917.3:p.Ser881=
ENST00000261917.3:c.2643C>A ENSP00000261917.3:p.Ser881=
NM_005477.2:c.2643C>A NP_005468.1:p.Ser881=
XM_011521148.1:c.1425C>A XP_011519450.1:p.Ser475=
XM_011521148.2:c.1425C>A XP_011519450.1:p.Ser475=
NM_005477.3:c.2643C>A MANE Select NP_005468.1:p.Ser881=