Canonical Allele Identifier: CA491152525
Gene: HCN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.73624484G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73332143G>T , CM000677.2:g.73332143G>T GRCh38
NC_000015.9:g.73624484G>T , CM000677.1:g.73624484G>T GRCh37
NC_000015.8:g.71411537G>T NCBI36
NG_009063.1:g.42122C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.1359C>A MANE Select ENSP00000261917.3:p.Ile453=
ENST00000261917.3:c.1359C>A ENSP00000261917.3:p.Ile453=
NM_005477.2:c.1359C>A NP_005468.1:p.Ile453=
XM_011521148.1:c.141C>A XP_011519450.1:p.Ile47=
XM_011521148.2:c.141C>A XP_011519450.1:p.Ile47=
NM_005477.3:c.1359C>A MANE Select NP_005468.1:p.Ile453=