Canonical Allele Identifier: CA491479297
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs2151228552
MyVariant Identifiers: chr15:g.73660198G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367857G>T , CM000677.2:g.73367857G>T GRCh38
NC_000015.9:g.73660198G>T , CM000677.1:g.73660198G>T GRCh37
NC_000015.8:g.71447251G>T NCBI36
NG_009063.1:g.6408C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.414C>A MANE Select ENSP00000261917.3:p.Ser138=
ENST00000261917.3:c.414C>A ENSP00000261917.3:p.Ser138=
NM_005477.2:c.414C>A NP_005468.1:p.Ser138=
NM_005477.3:c.414C>A MANE Select NP_005468.1:p.Ser138=