Canonical Allele Identifier: CA1937420405
Gene: HABP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.113570889T= , CM000672.2:g.113570889T= GRCh38
NC_000010.10:g.115330648T= , CM000672.1:g.115330648T= GRCh37
NC_000010.9:g.115320638T= NCBI36
NG_008956.1:g.22871T=

Transcript Alleles

HGVS Amino-acid change
ENST00000351270.4:c.106+3364T= MANE Select ENSP00000277903.4:n.106+3364T=
ENST00000351270.3:c.106+3364T= ENSP00000277903.4:n.106+3364T=
ENST00000542051.5:c.28+3364T= ENSP00000443283.1:n.28+3364T=
NM_001177660.1:c.28+3364T= NP_001171131.1:n.28+3364T=
NM_004132.3:c.106+3364T= NP_004123.1:n.106+3364T=
NM_001177660.2:c.28+3364T= NP_001171131.1:n.28+3364T=
NM_004132.4:c.106+3364T= NP_004123.1:n.106+3364T=
NM_004132.5:c.106+3364T= MANE Select NP_004123.1:n.106+3364T=
NM_001177660.3:c.28+3364T= NP_001171131.1:n.28+3364T=