Canonical Allele Identifier: CA196807544

Gene: GABBR2

Linked Data

• dbSNP Id: rs1024884770
• MyVariant Identifiers: chr9:g.101103666_101103668del (hg19) ; chr9:g.98341384_98341386del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.98341386_98341388del , CM000671.2:g.98341386_98341388del	GRCh38
NC_000009.11:g.101103668_101103670del , CM000671.1:g.101103668_101103670del	GRCh37
NC_000009.10:g.100143489_100143491del	NCBI36
NG_016426.1:g.372812_372814del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000259455.4:c.1893+21329_1893+21331del MANE Select	ENSP00000259455.2:n.1893+21329_1893+21331del
ENST00000637410.1:n.1671+21329_1671+21331del
ENST00000259455.3:c.1893+21329_1893+21331del	ENSP00000259455.2:n.1893+21329_1893+21331del
ENST00000634457.1:c.231+21329_231+21331del	ENSP00000489352.1:n.231+21329_231+21331del
ENST00000635462.1:n.388+21329_388+21331del
NM_005458.7:c.1893+21329_1893+21331del	NP_005449.5:n.1893+21329_1893+21331del
XM_005252316.3:c.1119+21329_1119+21331del	XP_005252373.1:n.1119+21329_1119+21331del
XM_005252316.5:c.1119+21329_1119+21331del	XP_005252373.1:n.1119+21329_1119+21331del
XM_017015331.2:c.1599+21329_1599+21331del	XP_016870820.1:n.1599+21329_1599+21331del
XM_017015332.2:c.1119+21329_1119+21331del	XP_016870821.1:n.1119+21329_1119+21331del
NM_005458.8:c.1893+21329_1893+21331del MANE Select	NP_005449.5:n.1893+21329_1893+21331del