Canonical Allele Identifier: CA5694079

Gene: HABP2

Linked Data

• dbSNP Id: rs764972183
• ExAC: 10:115348004 C / G
• gnomAD v3: 10-113588245-C-G
• gnomAD v4: 10-113588245-C-G
• MyVariant Identifiers: chr10:g.115348004C>G (hg19) ; chr10:g.113588245C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.113588245C>G , CM000672.2:g.113588245C>G	GRCh38
NC_000010.10:g.115348004C>G , CM000672.1:g.115348004C>G	GRCh37
NC_000010.9:g.115337994C>G	NCBI36
NG_008956.1:g.40227C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351270.4:c.1559C>G MANE Select	ENSP00000277903.4:p.Thr520Ser
ENST00000351270.3:c.1559C>G	ENSP00000277903.4:p.Thr520Ser
ENST00000542051.5:c.1481C>G	ENSP00000443283.1:p.Thr494Ser
NM_001177660.1:c.1481C>G	NP_001171131.1:p.Thr494Ser
NM_004132.3:c.1559C>G	NP_004123.1:p.Thr520Ser
NM_001177660.2:c.1481C>G	NP_001171131.1:p.Thr494Ser
NM_004132.4:c.1559C>G	NP_004123.1:p.Thr520Ser
NM_004132.5:c.1559C>G MANE Select	NP_004123.1:p.Thr520Ser
NM_001177660.3:c.1481C>G	NP_001171131.1:p.Thr494Ser