Canonical Allele Identifier: CA1984650260
Gene: GAB2 HGNC NCBI

Linked Data

dbSNP Id: rs2292573
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.78342093A>T , CM000673.2:g.78342093A>T GRCh38
NC_000011.9:g.78053139A>T , CM000673.1:g.78053139A>T GRCh37
NC_000011.8:g.77730787A>T NCBI36
NG_016171.1:g.80730T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000361507.5:c.76-61192T>A MANE Select ENSP00000354952.4:n.76-61192T>A
ENST00000361507.4:c.76-61192T>A ENSP00000354952.4:n.76-61192T>A
ENST00000526030.1:n.178-23874T>A
ENST00000528886.5:c.-39-61192T>A ENSP00000433762.1:n.-39-61192T>A
ENST00000530915.1:c.-40+21923T>A ENSP00000431868.1:n.-40+21923T>A
ENST00000534823.1:n.127-61192T>A
NM_080491.2:c.76-61192T>A NP_536739.1:n.76-61192T>A
XM_006718753.1:c.-40+21923T>A XP_006718816.1:n.-40+21923T>A
XM_006718753.2:c.-40+21923T>A XP_006718816.1:n.-40+21923T>A
XM_024448782.1:c.21+12641T>A XP_024304550.1:n.21+12641T>A
NM_080491.3:c.76-61192T>A MANE Select NP_536739.1:n.76-61192T>A
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