Canonical Allele Identifier: CA491479612
Gene: HCN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.73660123G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367782G>C , CM000677.2:g.73367782G>C GRCh38
NC_000015.9:g.73660123G>C , CM000677.1:g.73660123G>C GRCh37
NC_000015.8:g.71447176G>C NCBI36
NG_009063.1:g.6483C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.489C>G MANE Select ENSP00000261917.3:p.Ala163=
ENST00000261917.3:c.489C>G ENSP00000261917.3:p.Ala163=
NM_005477.2:c.489C>G NP_005468.1:p.Ala163=
NM_005477.3:c.489C>G MANE Select NP_005468.1:p.Ala163=