Canonical Allele Identifier: CA660073103
Gene: HABP2 HGNC NCBI

Linked Data

dbSNP Id: rs1477544490
gnomAD v4: 10-113588539-T-C
MyVariant Identifiers: chr10:g.115348298T>C (hg19) chr10:g.113588539T>C (hg38)
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Genomic Alleles

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

Transcript Alleles

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