Canonical Allele Identifier: CA491478126
Gene: HCN4 HGNC NCBI

Linked Data

gnomAD v4: 15-73323012-G-T
MyVariant Identifiers: chr15:g.73615353G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323012G>T , CM000677.2:g.73323012G>T GRCh38
NC_000015.9:g.73615353G>T , CM000677.1:g.73615353G>T GRCh37
NC_000015.8:g.71402406G>T NCBI36
NG_009063.1:g.51253C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3081C>A MANE Select ENSP00000261917.3:p.Pro1027=
ENST00000261917.3:c.3081C>A ENSP00000261917.3:p.Pro1027=
NM_005477.2:c.3081C>A NP_005468.1:p.Pro1027=
XM_011521148.1:c.1863C>A XP_011519450.1:p.Pro621=
XM_011521148.2:c.1863C>A XP_011519450.1:p.Pro621=
NM_005477.3:c.3081C>A MANE Select NP_005468.1:p.Pro1027=
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