Canonical Allele Identifier: CA1937420369
Gene: HABP2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.113570822T= , CM000672.2:g.113570822T= GRCh38
NC_000010.10:g.115330581T= , CM000672.1:g.115330581T= GRCh37
NC_000010.9:g.115320571T= NCBI36
NG_008956.1:g.22804T=

Transcript Alleles

HGVS Amino-acid change
ENST00000351270.4:c.106+3297T= MANE Select ENSP00000277903.4:n.106+3297T=
ENST00000351270.3:c.106+3297T= ENSP00000277903.4:n.106+3297T=
ENST00000542051.5:c.28+3297T= ENSP00000443283.1:n.28+3297T=
NM_001177660.1:c.28+3297T= NP_001171131.1:n.28+3297T=
NM_004132.3:c.106+3297T= NP_004123.1:n.106+3297T=
NM_001177660.2:c.28+3297T= NP_001171131.1:n.28+3297T=
NM_004132.4:c.106+3297T= NP_004123.1:n.106+3297T=
NM_004132.5:c.106+3297T= MANE Select NP_004123.1:n.106+3297T=
NM_001177660.3:c.28+3297T= NP_001171131.1:n.28+3297T=
Search 100 bp 5'
Search 100 bp 3'