Canonical Allele Identifier: CA1937429090

Gene: HABP2

Linked Data

• dbSNP Id: rs1845692374
• gnomAD v4: 10-113588144-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.113588149dup , CM000672.2:g.113588149dup	GRCh38
NC_000010.10:g.115347908dup , CM000672.1:g.115347908dup	GRCh37
NC_000010.9:g.115337898dup	NCBI36
NG_008956.1:g.40131dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351270.4:c.1519-56dup MANE Select	ENSP00000277903.4:n.1519-56dup
ENST00000351270.3:c.1519-56dup	ENSP00000277903.4:n.1519-56dup
ENST00000542051.5:c.1441-56dup	ENSP00000443283.1:n.1441-56dup
NM_001177660.1:c.1441-56dup	NP_001171131.1:n.1441-56dup
NM_004132.3:c.1519-56dup	NP_004123.1:n.1519-56dup
NM_001177660.2:c.1441-56dup	NP_001171131.1:n.1441-56dup
NM_004132.4:c.1519-56dup	NP_004123.1:n.1519-56dup
NM_004132.5:c.1519-56dup MANE Select	NP_004123.1:n.1519-56dup
NM_001177660.3:c.1441-56dup	NP_001171131.1:n.1441-56dup