Canonical Allele Identifier: CA471516925
Gene: HABP2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.115348053G>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.113588294G>A , CM000672.2:g.113588294G>A GRCh38
NC_000010.10:g.115348053G>A , CM000672.1:g.115348053G>A GRCh37
NC_000010.9:g.115338043G>A NCBI36
NG_008956.1:g.40276G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000351270.4:c.1608G>A MANE Select ENSP00000277903.4:p.Arg536=
ENST00000351270.3:c.1608G>A ENSP00000277903.4:p.Arg536=
ENST00000542051.5:c.1530G>A ENSP00000443283.1:p.Arg510=
NM_001177660.1:c.1530G>A NP_001171131.1:p.Arg510=
NM_004132.3:c.1608G>A NP_004123.1:p.Arg536=
NM_001177660.2:c.1530G>A NP_001171131.1:p.Arg510=
NM_004132.4:c.1608G>A NP_004123.1:p.Arg536=
NM_004132.5:c.1608G>A MANE Select NP_004123.1:p.Arg536=
NM_001177660.3:c.1530G>A NP_001171131.1:p.Arg510=
Search 100 bp 5'
Search 100 bp 3'