Canonical Allele Identifier: CA1937419472
Gene: HABP2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.113569140T= , CM000672.2:g.113569140T= GRCh38
NC_000010.10:g.115328899T= , CM000672.1:g.115328899T= GRCh37
NC_000010.9:g.115318889T= NCBI36
NG_008956.1:g.21122T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000351270.4:c.106+1615T= MANE Select ENSP00000277903.4:n.106+1615T=
ENST00000351270.3:c.106+1615T= ENSP00000277903.4:n.106+1615T=
ENST00000460714.1:n.43-504T=
ENST00000542051.5:c.28+1615T= ENSP00000443283.1:n.28+1615T=
NM_001177660.1:c.28+1615T= NP_001171131.1:n.28+1615T=
NM_004132.3:c.106+1615T= NP_004123.1:n.106+1615T=
NM_001177660.2:c.28+1615T= NP_001171131.1:n.28+1615T=
NM_004132.4:c.106+1615T= NP_004123.1:n.106+1615T=
NM_004132.5:c.106+1615T= MANE Select NP_004123.1:n.106+1615T=
NM_001177660.3:c.28+1615T= NP_001171131.1:n.28+1615T=
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