Canonical Allele Identifier: CA491151457
Gene: HCN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.73621935G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329594G>A , CM000677.2:g.73329594G>A GRCh38
NC_000015.9:g.73621935G>A , CM000677.1:g.73621935G>A GRCh37
NC_000015.8:g.71408988G>A NCBI36
NG_009063.1:g.44671C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.1569C>T MANE Select ENSP00000261917.3:p.Ser523=
ENST00000261917.3:c.1569C>T ENSP00000261917.3:p.Ser523=
NM_005477.2:c.1569C>T NP_005468.1:p.Ser523=
XM_011521148.1:c.351C>T XP_011519450.1:p.Ser117=
XM_011521148.2:c.351C>T XP_011519450.1:p.Ser117=
NM_005477.3:c.1569C>T MANE Select NP_005468.1:p.Ser523=