Canonical Allele Identifier: CA491479290
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1432463
dbSNP Id: rs1044205586
MyVariant Identifiers: chr15:g.73660192G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367851G>A , CM000677.2:g.73367851G>A GRCh38
NC_000015.9:g.73660192G>A , CM000677.1:g.73660192G>A GRCh37
NC_000015.8:g.71447245G>A NCBI36
NG_009063.1:g.6414C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.420C>T MANE Select ENSP00000261917.3:p.Gly140=
ENST00000261917.3:c.420C>T ENSP00000261917.3:p.Gly140=
NM_005477.2:c.420C>T NP_005468.1:p.Gly140=
NM_005477.3:c.420C>T MANE Select NP_005468.1:p.Gly140=