Canonical Allele Identifier: CA515419260

Gene: MBTPS2

Linked Data

• MyVariant Identifiers: chrX:g.21863337T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.21845219T>C , CM000685.2:g.21845219T>C	GRCh38
NC_000023.10:g.21863337T>C , CM000685.1:g.21863337T>C	GRCh37
NC_000023.9:g.21773258T>C	NCBI36
NG_012797.1:g.10682T>C
NG_012797.2:g.10682T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379484.10:c.273T>C MANE Select	ENSP00000368798.5:p.Phe91=
ENST00000365779.2:c.273T>C	ENSP00000368796.1:p.Phe91=
ENST00000379484.9:c.273T>C	ENSP00000368798.5:p.Phe91=
ENST00000465888.1:n.372T>C
NM_015884.3:c.273T>C	NP_056968.1:p.Phe91=
NM_015884.4:c.273T>C MANE Select	NP_056968.1:p.Phe91=