Canonical Allele Identifier: CA533379846

Gene: SPRED2

Linked Data

• dbSNP Id: rs937951378
• gnomAD v2: 2-65608986-G-A
• gnomAD v3: 2-65381852-G-A
• gnomAD v4: 2-65381852-G-A
• MyVariant Identifiers: chr2:g.65608986G>A (hg19) ; chr2:g.65381852G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.65381852G>A , CM000664.2:g.65381852G>A	GRCh38
NC_000002.11:g.65608986G>A , CM000664.1:g.65608986G>A	GRCh37
NC_000002.10:g.65462490G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356388.9:c.27-36956C>T MANE Select	ENSP00000348753.4:n.27-36956C>T
ENST00000356388.8:c.27-36956C>T	ENSP00000348753.4:n.27-36956C>T
ENST00000440972.1:c.27-36956C>T	ENSP00000406481.1:n.27-36956C>T
NM_181784.2:c.27-36956C>T	NP_861449.2:n.27-36956C>T
XM_005264200.3:c.27-36956C>T	XP_005264257.2:n.27-36956C>T
XM_005264202.3:c.27-36956C>T	XP_005264259.1:n.27-36956C>T
XM_006711966.1:c.27-36956C>T	XP_006712029.1:n.27-36956C>T
XM_005264200.5:c.27-36956C>T	XP_005264257.2:n.27-36956C>T
XM_005264202.5:c.27-36956C>T	XP_005264259.1:n.27-36956C>T
NM_181784.3:c.27-36956C>T MANE Select	NP_861449.2:n.27-36956C>T