Canonical Allele Identifier: CA491478213
Gene: HCN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.73615647C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323306C>T , CM000677.2:g.73323306C>T GRCh38
NC_000015.9:g.73615647C>T , CM000677.1:g.73615647C>T GRCh37
NC_000015.8:g.71402700C>T NCBI36
NG_009063.1:g.50959G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.2787G>A MANE Select ENSP00000261917.3:p.Leu929=
ENST00000261917.3:c.2787G>A ENSP00000261917.3:p.Leu929=
NM_005477.2:c.2787G>A NP_005468.1:p.Leu929=
XM_011521148.1:c.1569G>A XP_011519450.1:p.Leu523=
XM_011521148.2:c.1569G>A XP_011519450.1:p.Leu523=
NM_005477.3:c.2787G>A MANE Select NP_005468.1:p.Leu929=