Canonical Allele Identifier: CA11070498
Gene: SPRED2 HGNC NCBI

Linked Data

dbSNP Id: rs1876518
gnomAD v2: 2-65608909-C-T
gnomAD v3: 2-65381775-C-T
gnomAD v4: 2-65381775-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.65381775C>T , CM000664.2:g.65381775C>T GRCh38
NC_000002.11:g.65608909C>T , CM000664.1:g.65608909C>T GRCh37
NC_000002.10:g.65462413C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356388.9:c.27-36879G>A MANE Select ENSP00000348753.4:n.27-36879G>A
ENST00000356388.8:c.27-36879G>A ENSP00000348753.4:n.27-36879G>A
ENST00000440972.1:c.27-36879G>A ENSP00000406481.1:n.27-36879G>A
NM_181784.2:c.27-36879G>A NP_861449.2:n.27-36879G>A
XM_005264200.3:c.27-36879G>A XP_005264257.2:n.27-36879G>A
XM_005264202.3:c.27-36879G>A XP_005264259.1:n.27-36879G>A
XM_006711966.1:c.27-36879G>A XP_006712029.1:n.27-36879G>A
XM_005264200.5:c.27-36879G>A XP_005264257.2:n.27-36879G>A
XM_005264202.5:c.27-36879G>A XP_005264259.1:n.27-36879G>A
NM_181784.3:c.27-36879G>A MANE Select NP_861449.2:n.27-36879G>A