Canonical Allele Identifier: CA491152526
Gene: HCN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.73624487G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73332146G>C , CM000677.2:g.73332146G>C GRCh38
NC_000015.9:g.73624487G>C , CM000677.1:g.73624487G>C GRCh37
NC_000015.8:g.71411540G>C NCBI36
NG_009063.1:g.42119C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.1356C>G MANE Select ENSP00000261917.3:p.Ser452=
ENST00000261917.3:c.1356C>G ENSP00000261917.3:p.Ser452=
NM_005477.2:c.1356C>G NP_005468.1:p.Ser452=
XM_011521148.1:c.138C>G XP_011519450.1:p.Ser46=
XM_011521148.2:c.138C>G XP_011519450.1:p.Ser46=
NM_005477.3:c.1356C>G MANE Select NP_005468.1:p.Ser452=