Canonical Allele Identifier: CA2610952664
Gene: HABP2 HGNC NCBI

Linked Data

gnomAD v4: 10-113588633-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.113588633G>T , CM000672.2:g.113588633G>T GRCh38
NC_000010.10:g.115348392G>T , CM000672.1:g.115348392G>T GRCh37
NC_000010.9:g.115338382G>T NCBI36
NG_008956.1:g.40615G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000351270.4:c.*264G>T MANE Select ENSP00000277903.4:n.*264G>T
ENST00000351270.3:c.*264G>T ENSP00000277903.4:n.*264G>T
ENST00000542051.5:c.*264G>T ENSP00000443283.1:n.*264G>T
NM_001177660.1:c.*264G>T NP_001171131.1:n.*264G>T
NM_004132.3:c.*264G>T NP_004123.1:n.*264G>T
NM_001177660.2:c.*264G>T NP_001171131.1:n.*264G>T
NM_004132.4:c.*264G>T NP_004123.1:n.*264G>T
NM_004132.5:c.*264G>T MANE Select NP_004123.1:n.*264G>T
NM_001177660.3:c.*264G>T NP_001171131.1:n.*264G>T
Search 100 bp 5'
Search 100 bp 3'