Canonical Allele Identifier: CA1257217232
Gene: SPRED2 HGNC NCBI

Linked Data

dbSNP Id: rs1322999970
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.65381675C>G , CM000664.2:g.65381675C>G GRCh38
NC_000002.11:g.65608809C>G , CM000664.1:g.65608809C>G GRCh37
NC_000002.10:g.65462313C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356388.9:c.27-36779G>C MANE Select ENSP00000348753.4:n.27-36779G>C
ENST00000356388.8:c.27-36779G>C ENSP00000348753.4:n.27-36779G>C
ENST00000440972.1:c.27-36779G>C ENSP00000406481.1:n.27-36779G>C
NM_181784.2:c.27-36779G>C NP_861449.2:n.27-36779G>C
XM_005264200.3:c.27-36779G>C XP_005264257.2:n.27-36779G>C
XM_005264202.3:c.27-36779G>C XP_005264259.1:n.27-36779G>C
XM_006711966.1:c.27-36779G>C XP_006712029.1:n.27-36779G>C
XM_005264200.5:c.27-36779G>C XP_005264257.2:n.27-36779G>C
XM_005264202.5:c.27-36779G>C XP_005264259.1:n.27-36779G>C
NM_181784.3:c.27-36779G>C MANE Select NP_861449.2:n.27-36779G>C
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