Canonical Allele Identifier: CA471516922
Gene: HABP2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.115348050G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.113588291G>A , CM000672.2:g.113588291G>A GRCh38
NC_000010.10:g.115348050G>A , CM000672.1:g.115348050G>A GRCh37
NC_000010.9:g.115338040G>A NCBI36
NG_008956.1:g.40273G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000351270.4:c.1605G>A MANE Select ENSP00000277903.4:p.Lys535=
ENST00000351270.3:c.1605G>A ENSP00000277903.4:p.Lys535=
ENST00000542051.5:c.1527G>A ENSP00000443283.1:p.Lys509=
NM_001177660.1:c.1527G>A NP_001171131.1:p.Lys509=
NM_004132.3:c.1605G>A NP_004123.1:p.Lys535=
NM_001177660.2:c.1527G>A NP_001171131.1:p.Lys509=
NM_004132.4:c.1605G>A NP_004123.1:p.Lys535=
NM_004132.5:c.1605G>A MANE Select NP_004123.1:p.Lys535=
NM_001177660.3:c.1527G>A NP_001171131.1:p.Lys509=
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