Canonical Allele Identifier: CA771295499

Gene: SPRED2

Linked Data

• dbSNP Id: rs1380250801
• gnomAD v3: 2-65381875-C-G
• gnomAD v4: 2-65381875-C-G
• MyVariant Identifiers: chr2:g.65609009C>G (hg19) ; chr2:g.65381875C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.65381875C>G , CM000664.2:g.65381875C>G	GRCh38
NC_000002.11:g.65609009C>G , CM000664.1:g.65609009C>G	GRCh37
NC_000002.10:g.65462513C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356388.9:c.27-36979G>C MANE Select	ENSP00000348753.4:n.27-36979G>C
ENST00000356388.8:c.27-36979G>C	ENSP00000348753.4:n.27-36979G>C
ENST00000440972.1:c.27-36979G>C	ENSP00000406481.1:n.27-36979G>C
NM_181784.2:c.27-36979G>C	NP_861449.2:n.27-36979G>C
XM_005264200.3:c.27-36979G>C	XP_005264257.2:n.27-36979G>C
XM_005264202.3:c.27-36979G>C	XP_005264259.1:n.27-36979G>C
XM_006711966.1:c.27-36979G>C	XP_006712029.1:n.27-36979G>C
XM_005264200.5:c.27-36979G>C	XP_005264257.2:n.27-36979G>C
XM_005264202.5:c.27-36979G>C	XP_005264259.1:n.27-36979G>C
NM_181784.3:c.27-36979G>C MANE Select	NP_861449.2:n.27-36979G>C