Canonical Allele Identifier: CA1937429381
Gene: HABP2 HGNC NCBI

Linked Data

dbSNP Id: rs1845725589
gnomAD v4: 10-113588661-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.113588661A>G , CM000672.2:g.113588661A>G GRCh38
NC_000010.10:g.115348420A>G , CM000672.1:g.115348420A>G GRCh37
NC_000010.9:g.115338410A>G NCBI36
NG_008956.1:g.40643A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000351270.4:c.*292A>G MANE Select ENSP00000277903.4:n.*292A>G
ENST00000351270.3:c.*292A>G ENSP00000277903.4:n.*292A>G
ENST00000542051.5:c.*292A>G ENSP00000443283.1:n.*292A>G
NM_001177660.1:c.*292A>G NP_001171131.1:n.*292A>G
NM_004132.3:c.*292A>G NP_004123.1:n.*292A>G
NM_001177660.2:c.*292A>G NP_001171131.1:n.*292A>G
NM_004132.4:c.*292A>G NP_004123.1:n.*292A>G
NM_004132.5:c.*292A>G MANE Select NP_004123.1:n.*292A>G
NM_001177660.3:c.*292A>G NP_001171131.1:n.*292A>G
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