Canonical Allele Identifier: CA932724482

Gene: HABP2

Linked Data

• dbSNP Id: rs1845298441
• gnomAD v3: 10-113571067-T-A
• gnomAD v4: 10-113571067-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.113571067T>A , CM000672.2:g.113571067T>A	GRCh38
NC_000010.10:g.115330826T>A , CM000672.1:g.115330826T>A	GRCh37
NC_000010.9:g.115320816T>A	NCBI36
NG_008956.1:g.23049T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351270.4:c.107-3222T>A MANE Select	ENSP00000277903.4:n.107-3222T>A
ENST00000351270.3:c.107-3222T>A	ENSP00000277903.4:n.107-3222T>A
ENST00000542051.5:c.29-3222T>A	ENSP00000443283.1:n.29-3222T>A
NM_001177660.1:c.29-3222T>A	NP_001171131.1:n.29-3222T>A
NM_004132.3:c.107-3222T>A	NP_004123.1:n.107-3222T>A
NM_001177660.2:c.29-3222T>A	NP_001171131.1:n.29-3222T>A
NM_004132.4:c.107-3222T>A	NP_004123.1:n.107-3222T>A
NM_004132.5:c.107-3222T>A MANE Select	NP_004123.1:n.107-3222T>A
NM_001177660.3:c.29-3222T>A	NP_001171131.1:n.29-3222T>A