Canonical Allele Identifier: CA393086205
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322986C>A , CM000677.2:g.73322986C>A GRCh38
NC_000015.9:g.73615327C>A , CM000677.1:g.73615327C>A GRCh37
NC_000015.8:g.71402380C>A NCBI36
NG_009063.1:g.51279G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.3107G>T MANE Select ENSP00000261917.3:p.Arg1036Ile
ENST00000261917.3:c.3107G>T ENSP00000261917.3:p.Arg1036Ile
NM_005477.2:c.3107G>T NP_005468.1:p.Arg1036Ile
XM_011521148.1:c.1889G>T XP_011519450.1:p.Arg630Ile
XM_011521148.2:c.1889G>T XP_011519450.1:p.Arg630Ile
NM_005477.3:c.3107G>T MANE Select NP_005468.1:p.Arg1036Ile