Canonical Allele Identifier: CA2543797730
Gene: HABP2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.113570902C>A , CM000672.2:g.113570902C>A GRCh38
NC_000010.10:g.115330661C>A , CM000672.1:g.115330661C>A GRCh37
NC_000010.9:g.115320651C>A NCBI36
NG_008956.1:g.22884C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000351270.4:c.106+3377C>A MANE Select ENSP00000277903.4:n.106+3377C>A
ENST00000351270.3:c.106+3377C>A ENSP00000277903.4:n.106+3377C>A
ENST00000542051.5:c.28+3377C>A ENSP00000443283.1:n.28+3377C>A
NM_001177660.1:c.28+3377C>A NP_001171131.1:n.28+3377C>A
NM_004132.3:c.106+3377C>A NP_004123.1:n.106+3377C>A
NM_001177660.2:c.28+3377C>A NP_001171131.1:n.28+3377C>A
NM_004132.4:c.106+3377C>A NP_004123.1:n.106+3377C>A
NM_004132.5:c.106+3377C>A MANE Select NP_004123.1:n.106+3377C>A
NM_001177660.3:c.28+3377C>A NP_001171131.1:n.28+3377C>A
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