Canonical Allele Identifier: CA1937420409

Gene: HABP2

Linked Data

• dbSNP Id: rs1565101126

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.113570892A>G , CM000672.2:g.113570892A>G	GRCh38
NC_000010.10:g.115330651A>G , CM000672.1:g.115330651A>G	GRCh37
NC_000010.9:g.115320641A>G	NCBI36
NG_008956.1:g.22874A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000351270.4:c.106+3367A>G MANE Select	ENSP00000277903.4:n.106+3367A>G
ENST00000351270.3:c.106+3367A>G	ENSP00000277903.4:n.106+3367A>G
ENST00000542051.5:c.28+3367A>G	ENSP00000443283.1:n.28+3367A>G
NM_001177660.1:c.28+3367A>G	NP_001171131.1:n.28+3367A>G
NM_004132.3:c.106+3367A>G	NP_004123.1:n.106+3367A>G
NM_001177660.2:c.28+3367A>G	NP_001171131.1:n.28+3367A>G
NM_004132.4:c.106+3367A>G	NP_004123.1:n.106+3367A>G
NM_004132.5:c.106+3367A>G MANE Select	NP_004123.1:n.106+3367A>G
NM_001177660.3:c.28+3367A>G	NP_001171131.1:n.28+3367A>G