Canonical Allele Identifier: CA1937420373
Gene: HABP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.113570829C= , CM000672.2:g.113570829C= GRCh38
NC_000010.10:g.115330588C= , CM000672.1:g.115330588C= GRCh37
NC_000010.9:g.115320578C= NCBI36
NG_008956.1:g.22811C=

Transcript Alleles

HGVS Amino-acid change
ENST00000351270.4:c.106+3304C= MANE Select ENSP00000277903.4:n.106+3304C=
ENST00000351270.3:c.106+3304C= ENSP00000277903.4:n.106+3304C=
ENST00000542051.5:c.28+3304C= ENSP00000443283.1:n.28+3304C=
NM_001177660.1:c.28+3304C= NP_001171131.1:n.28+3304C=
NM_004132.3:c.106+3304C= NP_004123.1:n.106+3304C=
NM_001177660.2:c.28+3304C= NP_001171131.1:n.28+3304C=
NM_004132.4:c.106+3304C= NP_004123.1:n.106+3304C=
NM_004132.5:c.106+3304C= MANE Select NP_004123.1:n.106+3304C=
NM_001177660.3:c.28+3304C= NP_001171131.1:n.28+3304C=