Canonical Allele Identifier: CA1937429089

Gene: HABP2

Linked Data

• dbSNP Id: rs984101623
• gnomAD v4: 10-113588145-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.113588145G>A , CM000672.2:g.113588145G>A	GRCh38
NC_000010.10:g.115347904G>A , CM000672.1:g.115347904G>A	GRCh37
NC_000010.9:g.115337894G>A	NCBI36
NG_008956.1:g.40127G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351270.4:c.1519-60G>A MANE Select	ENSP00000277903.4:n.1519-60G>A
ENST00000351270.3:c.1519-60G>A	ENSP00000277903.4:n.1519-60G>A
ENST00000542051.5:c.1441-60G>A	ENSP00000443283.1:n.1441-60G>A
NM_001177660.1:c.1441-60G>A	NP_001171131.1:n.1441-60G>A
NM_004132.3:c.1519-60G>A	NP_004123.1:n.1519-60G>A
NM_001177660.2:c.1441-60G>A	NP_001171131.1:n.1441-60G>A
NM_004132.4:c.1519-60G>A	NP_004123.1:n.1519-60G>A
NM_004132.5:c.1519-60G>A MANE Select	NP_004123.1:n.1519-60G>A
NM_001177660.3:c.1441-60G>A	NP_001171131.1:n.1441-60G>A