Canonical Allele Identifier: CA491151527
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs1262596735
gnomAD v2: 15-73622001-C-A
gnomAD v4: 15-73329660-C-A
MyVariant Identifiers: chr15:g.73622001C>A (hg19) chr15:g.73329660C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329660C>A , CM000677.2:g.73329660C>A GRCh38
NC_000015.9:g.73622001C>A , CM000677.1:g.73622001C>A GRCh37
NC_000015.8:g.71409054C>A NCBI36
NG_009063.1:g.44605G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.1503G>T MANE Select ENSP00000261917.3:p.Val501=
ENST00000261917.3:c.1503G>T ENSP00000261917.3:p.Val501=
NM_005477.2:c.1503G>T NP_005468.1:p.Val501=
XM_011521148.1:c.285G>T XP_011519450.1:p.Val95=
XM_011521148.2:c.285G>T XP_011519450.1:p.Val95=
NM_005477.3:c.1503G>T MANE Select NP_005468.1:p.Val501=
Search 100 bp 5'
Search 100 bp 3'