Canonical Allele Identifier: CA449779163

Gene: VARS2

Linked Data

• MyVariant Identifiers: chr6:g.30890951T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30923174T>C , CM000668.2:g.30923174T>C	GRCh38
NC_000006.11:g.30890951T>C , CM000668.1:g.30890951T>C	GRCh37
NC_000006.10:g.30998930T>C	NCBI36
NG_034224.1:g.13967T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541562.6:c.2256T>C	ENSP00000441000.2:p.Ala752=
ENST00000672801.1:c.2250T>C	ENSP00000500615.1:p.Ala750=
ENST00000676266.1:c.2256T>C MANE Select	ENSP00000502585.1:p.Ala752=
ENST00000321897.9:c.2256T>C	ENSP00000316092.5:p.Ala752=
ENST00000469358.5:n.2244T>C
ENST00000476162.5:n.1043T>C
ENST00000477052.1:n.342T>C
ENST00000477288.5:n.4869T>C
ENST00000541562.5:c.2346T>C	ENSP00000441000.1:p.Ala782=
ENST00000542001.5:c.2250T>C	ENSP00000438200.2:p.Ala750=
ENST00000625423.2:c.1836T>C	ENSP00000485818.1:p.Ala612=
NM_001167733.2:c.1836T>C	NP_001161205.1:p.Ala612=
NM_001167734.1:c.2346T>C	NP_001161206.1:p.Ala782=
NM_020442.5:c.2256T>C	NP_065175.4:p.Ala752=
NM_001167733.3:c.1836T>C	NP_001161205.1:p.Ala612=
NM_001167734.2:c.2346T>C	NP_001161206.1:p.Ala782=
NM_020442.6:c.2256T>C MANE Select	NP_065175.4:p.Ala752=