Canonical Allele Identifier: CA347679265

Gene: SNRNP200

Linked Data

• MyVariant Identifiers: chr2:g.96958764C>A (hg19) ; chr2:g.96293026C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96293026C>A , CM000664.2:g.96293026C>A	GRCh38
NC_000002.11:g.96958764C>A , CM000664.1:g.96958764C>A	GRCh37
NC_000002.10:g.96322491C>A	NCBI36
NG_016973.1:g.17534G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323853.10:c.2106G>T MANE Select	ENSP00000317123.5:p.Gln702His
ENST00000652267.1:c.2106G>T	ENSP00000498933.1:p.Gln702His
ENST00000323853.9:c.2106G>T	ENSP00000317123.5:p.Gln702His
NM_014014.4:c.2106G>T	NP_054733.2:p.Gln702His
NM_014014.5:c.2106G>T MANE Select	NP_054733.2:p.Gln702His