Canonical Allele Identifier: CA471516955
Gene: HABP2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.115348059G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.113588300G>C , CM000672.2:g.113588300G>C GRCh38
NC_000010.10:g.115348059G>C , CM000672.1:g.115348059G>C GRCh37
NC_000010.9:g.115338049G>C NCBI36
NG_008956.1:g.40282G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000351270.4:c.1614G>C MANE Select ENSP00000277903.4:p.Gly538=
ENST00000351270.3:c.1614G>C ENSP00000277903.4:p.Gly538=
ENST00000542051.5:c.1536G>C ENSP00000443283.1:p.Gly512=
NM_001177660.1:c.1536G>C NP_001171131.1:p.Gly512=
NM_004132.3:c.1614G>C NP_004123.1:p.Gly538=
NM_001177660.2:c.1536G>C NP_001171131.1:p.Gly512=
NM_004132.4:c.1614G>C NP_004123.1:p.Gly538=
NM_004132.5:c.1614G>C MANE Select NP_004123.1:p.Gly538=
NM_001177660.3:c.1536G>C NP_001171131.1:p.Gly512=
Search 100 bp 5'
Search 100 bp 3'