Canonical Allele Identifier: CA378422089

Gene: HABP2

Linked Data

• MyVariant Identifiers: chr10:g.115348022T>G (hg19) ; chr10:g.113588263T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.113588263T>G , CM000672.2:g.113588263T>G	GRCh38
NC_000010.10:g.115348022T>G , CM000672.1:g.115348022T>G	GRCh37
NC_000010.9:g.115338012T>G	NCBI36
NG_008956.1:g.40245T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351270.4:c.1577T>G MANE Select	ENSP00000277903.4:p.Ile526Arg
ENST00000351270.3:c.1577T>G	ENSP00000277903.4:p.Ile526Arg
ENST00000542051.5:c.1499T>G	ENSP00000443283.1:p.Ile500Arg
NM_001177660.1:c.1499T>G	NP_001171131.1:p.Ile500Arg
NM_004132.3:c.1577T>G	NP_004123.1:p.Ile526Arg
NM_001177660.2:c.1499T>G	NP_001171131.1:p.Ile500Arg
NM_004132.4:c.1577T>G	NP_004123.1:p.Ile526Arg
NM_004132.5:c.1577T>G MANE Select	NP_004123.1:p.Ile526Arg
NM_001177660.3:c.1499T>G	NP_001171131.1:p.Ile500Arg