Canonical Allele Identifier: CA214443986
Gene: HABP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 879492
ClinVar RCV Id: RCV001107042
dbSNP Id: rs771345114
gnomAD v2: 10-115348283-T-A
gnomAD v3: 10-113588524-T-A
gnomAD v4: 10-113588524-T-A
MyVariant Identifiers: chr10:g.115348283T>A (hg19) chr10:g.113588524T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.113588524T>A , CM000672.2:g.113588524T>A GRCh38
NC_000010.10:g.115348283T>A , CM000672.1:g.115348283T>A GRCh37
NC_000010.9:g.115338273T>A NCBI36
NG_008956.1:g.40506T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000351270.4:c.*155T>A MANE Select ENSP00000277903.4:n.*155T>A
ENST00000351270.3:c.*155T>A ENSP00000277903.4:n.*155T>A
ENST00000542051.5:c.*155T>A ENSP00000443283.1:n.*155T>A
NM_001177660.1:c.*155T>A NP_001171131.1:n.*155T>A
NM_004132.3:c.*155T>A NP_004123.1:n.*155T>A
NM_001177660.2:c.*155T>A NP_001171131.1:n.*155T>A
NM_004132.4:c.*155T>A NP_004123.1:n.*155T>A
NM_004132.5:c.*155T>A MANE Select NP_004123.1:n.*155T>A
NM_001177660.3:c.*155T>A NP_001171131.1:n.*155T>A
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Search 100 bp 3'