Canonical Allele Identifier: CA49368535

Gene: SPRED2

Linked Data

• dbSNP Id: rs931169755
• gnomAD v2: 2-65608419-T-C
• gnomAD v3: 2-65381285-T-C
• gnomAD v4: 2-65381285-T-C
• MyVariant Identifiers: chr2:g.65608419T>C (hg19) ; chr2:g.65381285T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.65381285T>C , CM000664.2:g.65381285T>C	GRCh38
NC_000002.11:g.65608419T>C , CM000664.1:g.65608419T>C	GRCh37
NC_000002.10:g.65461923T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356388.9:c.27-36389A>G MANE Select	ENSP00000348753.4:n.27-36389A>G
ENST00000356388.8:c.27-36389A>G	ENSP00000348753.4:n.27-36389A>G
ENST00000440972.1:c.27-36389A>G	ENSP00000406481.1:n.27-36389A>G
NM_181784.2:c.27-36389A>G	NP_861449.2:n.27-36389A>G
XM_005264200.3:c.27-36389A>G	XP_005264257.2:n.27-36389A>G
XM_005264202.3:c.27-36389A>G	XP_005264259.1:n.27-36389A>G
XM_006711966.1:c.27-36389A>G	XP_006712029.1:n.27-36389A>G
XM_005264200.5:c.27-36389A>G	XP_005264257.2:n.27-36389A>G
XM_005264202.5:c.27-36389A>G	XP_005264259.1:n.27-36389A>G
NM_181784.3:c.27-36389A>G MANE Select	NP_861449.2:n.27-36389A>G