Canonical Allele Identifier: CA363175827

Gene: VARS2

Linked Data

• dbSNP Id: rs2150567055
• MyVariant Identifiers: chr6:g.30891263A>C (hg19) ; chr6:g.30923486A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30923486A>C , CM000668.2:g.30923486A>C	GRCh38
NC_000006.11:g.30891263A>C , CM000668.1:g.30891263A>C	GRCh37
NC_000006.10:g.30999242A>C	NCBI36
NG_034224.1:g.14279A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541562.6:c.2447A>C	ENSP00000441000.2:p.Asn816Thr
ENST00000672801.1:c.2441A>C	ENSP00000500615.1:p.Asn814Thr
ENST00000676266.1:c.2447A>C MANE Select	ENSP00000502585.1:p.Asn816Thr
ENST00000321897.9:c.2447A>C	ENSP00000316092.5:p.Asn816Thr
ENST00000469358.5:n.2435A>C
ENST00000473916.1:n.158A>C
ENST00000476162.5:n.1234A>C
ENST00000477052.1:n.533A>C
ENST00000477288.5:n.5060A>C
ENST00000541562.5:c.2537A>C	ENSP00000441000.1:p.Asn846Thr
ENST00000542001.5:c.2441A>C	ENSP00000438200.2:p.Asn814Thr
ENST00000625423.2:c.2027A>C	ENSP00000485818.1:p.Asn676Thr
NM_001167733.2:c.2027A>C	NP_001161205.1:p.Asn676Thr
NM_001167734.1:c.2537A>C	NP_001161206.1:p.Asn846Thr
NM_020442.5:c.2447A>C	NP_065175.4:p.Asn816Thr
NM_001167733.3:c.2027A>C	NP_001161205.1:p.Asn676Thr
NM_001167734.2:c.2537A>C	NP_001161206.1:p.Asn846Thr
NM_020442.6:c.2447A>C MANE Select	NP_065175.4:p.Asn816Thr