Canonical Allele Identifier: CA1338125875
Gene: ASB1 HGNC NCBI

Linked Data

dbSNP Id: rs1575006233

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.238440758A>G , CM000664.2:g.238440758A>G GRCh38
NC_000002.11:g.239349399A>G , CM000664.1:g.239349399A>G GRCh37
NC_000002.10:g.239014138A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000264607.9:c.495-3584A>G MANE Select ENSP00000264607.4:n.495-3584A>G
ENST00000264607.8:c.495-3584A>G ENSP00000264607.4:n.495-3584A>G
ENST00000409297.1:c.192-3584A>G ENSP00000387025.1:n.192-3584A>G
ENST00000438264.5:c.*167-3584A>G ENSP00000411773.1:n.*167-3584A>G
ENST00000463352.5:n.536-3584A>G
ENST00000468122.1:n.94-3584A>G
ENST00000491653.1:n.686-3584A>G
NM_001040445.1:c.495-3584A>G NP_001035535.1:n.495-3584A>G
XM_005246080.1:c.192-3584A>G XP_005246137.1:n.192-3584A>G
XR_241236.1:n.825-3584A>G
XR_241237.1:n.825-3584A>G
NM_001040445.2:c.495-3584A>G NP_001035535.1:n.495-3584A>G
NM_001330196.1:c.192-3584A>G NP_001317125.1:n.192-3584A>G
NM_001040445.3:c.495-3584A>G MANE Select NP_001035535.1:n.495-3584A>G
NM_001330196.2:c.192-3584A>G NP_001317125.1:n.192-3584A>G