Canonical Allele Identifier: CA491479293
Gene: HCN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.73660195G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367854G>C , CM000677.2:g.73367854G>C GRCh38
NC_000015.9:g.73660195G>C , CM000677.1:g.73660195G>C GRCh37
NC_000015.8:g.71447248G>C NCBI36
NG_009063.1:g.6411C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.417C>G MANE Select ENSP00000261917.3:p.Pro139=
ENST00000261917.3:c.417C>G ENSP00000261917.3:p.Pro139=
NM_005477.2:c.417C>G NP_005468.1:p.Pro139=
NM_005477.3:c.417C>G MANE Select NP_005468.1:p.Pro139=