Canonical Allele Identifier: CA393085637
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs1384783760
gnomAD v2: 15-73615115-G-A
gnomAD v3: 15-73322774-G-A
gnomAD v4: 15-73322774-G-A
MyVariant Identifiers: chr15:g.73615115G>A (hg19) chr15:g.73322774G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322774G>A , CM000677.2:g.73322774G>A GRCh38
NC_000015.9:g.73615115G>A , CM000677.1:g.73615115G>A GRCh37
NC_000015.8:g.71402168G>A NCBI36
NG_009063.1:g.51491C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3319C>T MANE Select ENSP00000261917.3:p.His1107Tyr
ENST00000261917.3:c.3319C>T ENSP00000261917.3:p.His1107Tyr
NM_005477.2:c.3319C>T NP_005468.1:p.His1107Tyr
XM_011521148.1:c.2101C>T XP_011519450.1:p.His701Tyr
XM_011521148.2:c.2101C>T XP_011519450.1:p.His701Tyr
NM_005477.3:c.3319C>T MANE Select NP_005468.1:p.His1107Tyr
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