Canonical Allele Identifier: CA2610952602
Gene: HABP2 HGNC NCBI

Linked Data

gnomAD v4: 10-113588539-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.113588539T>A , CM000672.2:g.113588539T>A GRCh38
NC_000010.10:g.115348298T>A , CM000672.1:g.115348298T>A GRCh37
NC_000010.9:g.115338288T>A NCBI36
NG_008956.1:g.40521T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000351270.4:c.*170T>A MANE Select ENSP00000277903.4:n.*170T>A
ENST00000351270.3:c.*170T>A ENSP00000277903.4:n.*170T>A
ENST00000542051.5:c.*170T>A ENSP00000443283.1:n.*170T>A
NM_001177660.1:c.*170T>A NP_001171131.1:n.*170T>A
NM_004132.3:c.*170T>A NP_004123.1:n.*170T>A
NM_001177660.2:c.*170T>A NP_001171131.1:n.*170T>A
NM_004132.4:c.*170T>A NP_004123.1:n.*170T>A
NM_004132.5:c.*170T>A MANE Select NP_004123.1:n.*170T>A
NM_001177660.3:c.*170T>A NP_001171131.1:n.*170T>A
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