Canonical Allele Identifier: CA2838666070
Gene: GAB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.78380103G>A , CM000673.2:g.78380103G>A GRCh38
NC_000011.9:g.78091149G>A , CM000673.1:g.78091149G>A GRCh37
NC_000011.8:g.77768797G>A NCBI36
NG_016171.1:g.42720C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000361507.5:c.75+37543C>T MANE Select ENSP00000354952.4:n.75+37543C>T
ENST00000361507.4:c.75+37543C>T ENSP00000354952.4:n.75+37543C>T
ENST00000526030.1:n.177+37543C>T
ENST00000528886.5:c.-40+38134C>T ENSP00000433762.1:n.-40+38134C>T
ENST00000530915.1:c.-127-16000C>T ENSP00000431868.1:n.-127-16000C>T
ENST00000534823.1:n.126+37543C>T
NM_080491.2:c.75+37543C>T NP_536739.1:n.75+37543C>T
XM_006718753.1:c.-127-16000C>T XP_006718816.1:n.-127-16000C>T
XM_006718753.2:c.-127-16000C>T XP_006718816.1:n.-127-16000C>T
NM_080491.3:c.75+37543C>T MANE Select NP_536739.1:n.75+37543C>T