Canonical Allele Identifier: CA393086690
Gene: HCN4 HGNC NCBI

Linked Data

gnomAD v4: 15-73323139-C-A
MyVariant Identifiers: chr15:g.73615480C>A (hg19) chr15:g.73323139C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323139C>A , CM000677.2:g.73323139C>A GRCh38
NC_000015.9:g.73615480C>A , CM000677.1:g.73615480C>A GRCh37
NC_000015.8:g.71402533C>A NCBI36
NG_009063.1:g.51126G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.2954G>T MANE Select ENSP00000261917.3:p.Gly985Val
ENST00000261917.3:c.2954G>T ENSP00000261917.3:p.Gly985Val
NM_005477.2:c.2954G>T NP_005468.1:p.Gly985Val
XM_011521148.1:c.1736G>T XP_011519450.1:p.Gly579Val
XM_011521148.2:c.1736G>T XP_011519450.1:p.Gly579Val
NM_005477.3:c.2954G>T MANE Select NP_005468.1:p.Gly985Val
Search 100 bp 5'
Search 100 bp 3'