Canonical Allele Identifier: CA11051276
Gene: ASB1 HGNC NCBI

Linked Data

dbSNP Id: rs3769124

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.238440721G>A , CM000664.2:g.238440721G>A GRCh38
NC_000002.11:g.239349362G>A , CM000664.1:g.239349362G>A GRCh37
NC_000002.10:g.239014101G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000264607.9:c.495-3621G>A MANE Select ENSP00000264607.4:p.=
ENST00000264607.8:c.495-3621G>A ENSP00000264607.4:p.=
ENST00000409297.1:c.192-3621G>A ENSP00000387025.1:p.=
ENST00000438264.5:c.*167-3621G>A ENSP00000411773.1:p.=
ENST00000463352.5:n.536-3621G>A
ENST00000468122.1:n.94-3621G>A
ENST00000491653.1:n.686-3621G>A
NM_001040445.1:c.495-3621G>A NP_001035535.1:p.=
XM_005246080.1:c.192-3621G>A XP_005246137.1:p.=
XR_241236.1:n.825-3621G>A
XR_241237.1:n.825-3621G>A
NM_001040445.2:c.495-3621G>A NP_001035535.1:p.=
NM_001330196.1:c.192-3621G>A NP_001317125.1:p.=
NM_001040445.3:c.495-3621G>A MANE Select NP_001035535.1:p.=
NM_001330196.2:c.192-3621G>A NP_001317125.1:p.=