Canonical Allele Identifier: CA214431650

Gene: HABP2

Linked Data

• dbSNP Id: rs370992048
• MyVariant Identifiers: chr10:g.115330663A>G (hg19) ; chr10:g.113570904A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.113570904A>G , CM000672.2:g.113570904A>G	GRCh38
NC_000010.10:g.115330663A>G , CM000672.1:g.115330663A>G	GRCh37
NC_000010.9:g.115320653A>G	NCBI36
NG_008956.1:g.22886A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351270.4:c.106+3379A>G MANE Select	ENSP00000277903.4:n.106+3379A>G
ENST00000351270.3:c.106+3379A>G	ENSP00000277903.4:n.106+3379A>G
ENST00000542051.5:c.28+3379A>G	ENSP00000443283.1:n.28+3379A>G
NM_001177660.1:c.28+3379A>G	NP_001171131.1:n.28+3379A>G
NM_004132.3:c.106+3379A>G	NP_004123.1:n.106+3379A>G
NM_001177660.2:c.28+3379A>G	NP_001171131.1:n.28+3379A>G
NM_004132.4:c.106+3379A>G	NP_004123.1:n.106+3379A>G
NM_004132.5:c.106+3379A>G MANE Select	NP_004123.1:n.106+3379A>G
NM_001177660.3:c.28+3379A>G	NP_001171131.1:n.28+3379A>G