Canonical Allele Identifier: CA2610952334

Gene: HABP2

Linked Data

• gnomAD v4: 10-113588078-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.113588078A>G , CM000672.2:g.113588078A>G	GRCh38
NC_000010.10:g.115347837A>G , CM000672.1:g.115347837A>G	GRCh37
NC_000010.9:g.115337827A>G	NCBI36
NG_008956.1:g.40060A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351270.4:c.1519-127A>G MANE Select	ENSP00000277903.4:n.1519-127A>G
ENST00000351270.3:c.1519-127A>G	ENSP00000277903.4:n.1519-127A>G
ENST00000542051.5:c.1441-127A>G	ENSP00000443283.1:n.1441-127A>G
NM_001177660.1:c.1441-127A>G	NP_001171131.1:n.1441-127A>G
NM_004132.3:c.1519-127A>G	NP_004123.1:n.1519-127A>G
NM_001177660.2:c.1441-127A>G	NP_001171131.1:n.1441-127A>G
NM_004132.4:c.1519-127A>G	NP_004123.1:n.1519-127A>G
NM_004132.5:c.1519-127A>G MANE Select	NP_004123.1:n.1519-127A>G
NM_001177660.3:c.1441-127A>G	NP_001171131.1:n.1441-127A>G