Canonical Allele Identifier: CA5694092
Gene: HABP2 HGNC NCBI

Linked Data

dbSNP Id: rs746994852

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.113588332G>A , CM000672.2:g.113588332G>A GRCh38
NC_000010.10:g.115348091G>A , CM000672.1:g.115348091G>A GRCh37
NC_000010.9:g.115338081G>A NCBI36
NG_008956.1:g.40314G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000351270.4:c.1646G>A MANE Select ENSP00000277903.4:p.Trp549Ter
ENST00000351270.3:c.1646G>A ENSP00000277903.4:p.Trp549Ter
ENST00000542051.5:c.1568G>A ENSP00000443283.1:p.Trp523Ter
NM_001177660.1:c.1568G>A NP_001171131.1:p.Trp523Ter
NM_004132.3:c.1646G>A NP_004123.1:p.Trp549Ter
NM_001177660.2:c.1568G>A NP_001171131.1:p.Trp523Ter
NM_004132.4:c.1646G>A NP_004123.1:p.Trp549Ter
NM_004132.5:c.1646G>A MANE Select NP_004123.1:p.Trp549Ter
NM_001177660.3:c.1568G>A NP_001171131.1:p.Trp523Ter