Canonical Allele Identifier: CA1937429070
Gene: HABP2 HGNC NCBI

Linked Data

dbSNP Id: rs1267098797
gnomAD v4: 10-113588112-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.113588112C>A , CM000672.2:g.113588112C>A GRCh38
NC_000010.10:g.115347871C>A , CM000672.1:g.115347871C>A GRCh37
NC_000010.9:g.115337861C>A NCBI36
NG_008956.1:g.40094C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000351270.4:c.1519-93C>A MANE Select ENSP00000277903.4:n.1519-93C>A
ENST00000351270.3:c.1519-93C>A ENSP00000277903.4:n.1519-93C>A
ENST00000542051.5:c.1441-93C>A ENSP00000443283.1:n.1441-93C>A
NM_001177660.1:c.1441-93C>A NP_001171131.1:n.1441-93C>A
NM_004132.3:c.1519-93C>A NP_004123.1:n.1519-93C>A
NM_001177660.2:c.1441-93C>A NP_001171131.1:n.1441-93C>A
NM_004132.4:c.1519-93C>A NP_004123.1:n.1519-93C>A
NM_004132.5:c.1519-93C>A MANE Select NP_004123.1:n.1519-93C>A
NM_001177660.3:c.1441-93C>A NP_001171131.1:n.1441-93C>A
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