Canonical Allele Identifier: CA491478123
Gene: HCN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.73615350A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323009A>T , CM000677.2:g.73323009A>T GRCh38
NC_000015.9:g.73615350A>T , CM000677.1:g.73615350A>T GRCh37
NC_000015.8:g.71402403A>T NCBI36
NG_009063.1:g.51256T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3084T>A MANE Select ENSP00000261917.3:p.Pro1028=
ENST00000261917.3:c.3084T>A ENSP00000261917.3:p.Pro1028=
NM_005477.2:c.3084T>A NP_005468.1:p.Pro1028=
XM_011521148.1:c.1866T>A XP_011519450.1:p.Pro622=
XM_011521148.2:c.1866T>A XP_011519450.1:p.Pro622=
NM_005477.3:c.3084T>A MANE Select NP_005468.1:p.Pro1028=
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