Canonical Allele Identifier: CA214431716
Gene: HABP2 HGNC NCBI

Linked Data

dbSNP Id: rs1054922939

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.113571073G>T , CM000672.2:g.113571073G>T GRCh38
NC_000010.10:g.115330832G>T , CM000672.1:g.115330832G>T GRCh37
NC_000010.9:g.115320822G>T NCBI36
NG_008956.1:g.23055G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000351270.4:c.107-3216G>T MANE Select ENSP00000277903.4:n.107-3216G>T
ENST00000351270.3:c.107-3216G>T ENSP00000277903.4:n.107-3216G>T
ENST00000542051.5:c.29-3216G>T ENSP00000443283.1:n.29-3216G>T
NM_001177660.1:c.29-3216G>T NP_001171131.1:n.29-3216G>T
NM_004132.3:c.107-3216G>T NP_004123.1:n.107-3216G>T
NM_001177660.2:c.29-3216G>T NP_001171131.1:n.29-3216G>T
NM_004132.4:c.107-3216G>T NP_004123.1:n.107-3216G>T
NM_004132.5:c.107-3216G>T MANE Select NP_004123.1:n.107-3216G>T
NM_001177660.3:c.29-3216G>T NP_001171131.1:n.29-3216G>T