Canonical Allele Identifier: CA2724455860
Gene: GAB2 HGNC NCBI

Linked Data

dbSNP Id: rs2134737494

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.78380015G>C , CM000673.2:g.78380015G>C GRCh38
NC_000011.9:g.78091061G>C , CM000673.1:g.78091061G>C GRCh37
NC_000011.8:g.77768709G>C NCBI36
NG_016171.1:g.42808C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000361507.5:c.75+37631C>G MANE Select ENSP00000354952.4:n.75+37631C>G
ENST00000361507.4:c.75+37631C>G ENSP00000354952.4:n.75+37631C>G
ENST00000526030.1:n.177+37631C>G
ENST00000528886.5:c.-40+38222C>G ENSP00000433762.1:n.-40+38222C>G
ENST00000530915.1:c.-127-15912C>G ENSP00000431868.1:n.-127-15912C>G
ENST00000534823.1:n.126+37631C>G
NM_080491.2:c.75+37631C>G NP_536739.1:n.75+37631C>G
XM_006718753.1:c.-127-15912C>G XP_006718816.1:n.-127-15912C>G
XM_006718753.2:c.-127-15912C>G XP_006718816.1:n.-127-15912C>G
NM_080491.3:c.75+37631C>G MANE Select NP_536739.1:n.75+37631C>G