Canonical Allele Identifier: CA2677910265

Gene: VARS2

Linked Data

• gnomAD v4: 6-30923504-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30923506del , CM000668.2:g.30923506del	GRCh38
NC_000006.11:g.30891283del , CM000668.1:g.30891283del	GRCh37
NC_000006.10:g.30999262del	NCBI36
NG_034224.1:g.14299del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541562.6:c.2466+1del
ENST00000672801.1:c.2460+1del
ENST00000676266.1:c.2466+1del
ENST00000321897.9:c.2466+1del
ENST00000469358.5:n.2454+1del
ENST00000473916.1:n.178del
ENST00000476162.5:n.1253+1del
ENST00000477288.5:n.5079+1del
ENST00000541562.5:c.2556+1del
ENST00000542001.5:c.2460+1del
ENST00000625423.2:c.2046+1del
NM_001167733.2:c.2046+1del
NM_001167734.1:c.2556+1del
NM_020442.5:c.2466+1del
NM_001167733.3:c.2046+1del
NM_001167734.2:c.2556+1del
NM_020442.6:c.2466+1del