Canonical Allele Identifier: CA1937420379
Gene: HABP2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.113570838C= , CM000672.2:g.113570838C= GRCh38
NC_000010.10:g.115330597C= , CM000672.1:g.115330597C= GRCh37
NC_000010.9:g.115320587C= NCBI36
NG_008956.1:g.22820C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000351270.4:c.106+3313C= MANE Select ENSP00000277903.4:n.106+3313C=
ENST00000351270.3:c.106+3313C= ENSP00000277903.4:n.106+3313C=
ENST00000542051.5:c.28+3313C= ENSP00000443283.1:n.28+3313C=
NM_001177660.1:c.28+3313C= NP_001171131.1:n.28+3313C=
NM_004132.3:c.106+3313C= NP_004123.1:n.106+3313C=
NM_001177660.2:c.28+3313C= NP_001171131.1:n.28+3313C=
NM_004132.4:c.106+3313C= NP_004123.1:n.106+3313C=
NM_004132.5:c.106+3313C= MANE Select NP_004123.1:n.106+3313C=
NM_001177660.3:c.28+3313C= NP_001171131.1:n.28+3313C=
Search 100 bp 5'
Search 100 bp 3'