Canonical Allele Identifier: CA471516924

Gene: HABP2

Linked Data

• gnomAD v4: 10-113588292-A-C
• MyVariant Identifiers: chr10:g.115348051A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.113588292A>C , CM000672.2:g.113588292A>C	GRCh38
NC_000010.10:g.115348051A>C , CM000672.1:g.115348051A>C	GRCh37
NC_000010.9:g.115338041A>C	NCBI36
NG_008956.1:g.40274A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000351270.4:c.1606A>C MANE Select	ENSP00000277903.4:p.Arg536=
ENST00000351270.3:c.1606A>C	ENSP00000277903.4:p.Arg536=
ENST00000542051.5:c.1528A>C	ENSP00000443283.1:p.Arg510=
NM_001177660.1:c.1528A>C	NP_001171131.1:p.Arg510=
NM_004132.3:c.1606A>C	NP_004123.1:p.Arg536=
NM_001177660.2:c.1528A>C	NP_001171131.1:p.Arg510=
NM_004132.4:c.1606A>C	NP_004123.1:p.Arg536=
NM_004132.5:c.1606A>C MANE Select	NP_004123.1:p.Arg536=
NM_001177660.3:c.1528A>C	NP_001171131.1:p.Arg510=