Canonical Allele Identifier: CA5694088
Gene: HABP2 HGNC NCBI

Linked Data

dbSNP Id: rs545620831
ExAC: 10:115348052 G / C
gnomAD v2: 10-115348052-G-C
gnomAD v3: 10-113588293-G-C
gnomAD v4: 10-113588293-G-C
MyVariant Identifiers: chr10:g.115348052G>C (hg19) chr10:g.113588293G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.113588293G>C , CM000672.2:g.113588293G>C GRCh38
NC_000010.10:g.115348052G>C , CM000672.1:g.115348052G>C GRCh37
NC_000010.9:g.115338042G>C NCBI36
NG_008956.1:g.40275G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000351270.4:c.1607G>C MANE Select ENSP00000277903.4:p.Arg536Thr
ENST00000351270.3:c.1607G>C ENSP00000277903.4:p.Arg536Thr
ENST00000542051.5:c.1529G>C ENSP00000443283.1:p.Arg510Thr
NM_001177660.1:c.1529G>C NP_001171131.1:p.Arg510Thr
NM_004132.3:c.1607G>C NP_004123.1:p.Arg536Thr
NM_001177660.2:c.1529G>C NP_001171131.1:p.Arg510Thr
NM_004132.4:c.1607G>C NP_004123.1:p.Arg536Thr
NM_004132.5:c.1607G>C MANE Select NP_004123.1:p.Arg536Thr
NM_001177660.3:c.1529G>C NP_001171131.1:p.Arg510Thr
Search 100 bp 5'
Search 100 bp 3'