Canonical Allele Identifier: CA2610952487
Gene: HABP2 HGNC NCBI

Linked Data

gnomAD v4: 10-113588438-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.113588438C>G , CM000672.2:g.113588438C>G GRCh38
NC_000010.10:g.115348197C>G , CM000672.1:g.115348197C>G GRCh37
NC_000010.9:g.115338187C>G NCBI36
NG_008956.1:g.40420C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000351270.4:c.*69C>G MANE Select ENSP00000277903.4:n.*69C>G
ENST00000351270.3:c.*69C>G ENSP00000277903.4:n.*69C>G
ENST00000542051.5:c.*69C>G ENSP00000443283.1:n.*69C>G
NM_001177660.1:c.*69C>G NP_001171131.1:n.*69C>G
NM_004132.3:c.*69C>G NP_004123.1:n.*69C>G
NM_001177660.2:c.*69C>G NP_001171131.1:n.*69C>G
NM_004132.4:c.*69C>G NP_004123.1:n.*69C>G
NM_004132.5:c.*69C>G MANE Select NP_004123.1:n.*69C>G
NM_001177660.3:c.*69C>G NP_001171131.1:n.*69C>G
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