Canonical Allele Identifier: CA2610952575
Gene: HABP2 HGNC NCBI

Linked Data

gnomAD v4: 10-113588516-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.113588516C>A , CM000672.2:g.113588516C>A GRCh38
NC_000010.10:g.115348275C>A , CM000672.1:g.115348275C>A GRCh37
NC_000010.9:g.115338265C>A NCBI36
NG_008956.1:g.40498C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000351270.4:c.*147C>A MANE Select ENSP00000277903.4:n.*147C>A
ENST00000351270.3:c.*147C>A ENSP00000277903.4:n.*147C>A
ENST00000542051.5:c.*147C>A ENSP00000443283.1:n.*147C>A
NM_001177660.1:c.*147C>A NP_001171131.1:n.*147C>A
NM_004132.3:c.*147C>A NP_004123.1:n.*147C>A
NM_001177660.2:c.*147C>A NP_001171131.1:n.*147C>A
NM_004132.4:c.*147C>A NP_004123.1:n.*147C>A
NM_004132.5:c.*147C>A MANE Select NP_004123.1:n.*147C>A
NM_001177660.3:c.*147C>A NP_001171131.1:n.*147C>A
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