Canonical Allele Identifier: CA533379843
Gene: SPRED2 HGNC NCBI

Linked Data

dbSNP Id: rs1402617661
gnomAD v2: 2-65608958-T-G
gnomAD v3: 2-65381824-T-G
gnomAD v4: 2-65381824-T-G
MyVariant Identifiers: chr2:g.65608958T>G (hg19) chr2:g.65381824T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.65381824T>G , CM000664.2:g.65381824T>G GRCh38
NC_000002.11:g.65608958T>G , CM000664.1:g.65608958T>G GRCh37
NC_000002.10:g.65462462T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356388.9:c.27-36928A>C MANE Select ENSP00000348753.4:n.27-36928A>C
ENST00000356388.8:c.27-36928A>C ENSP00000348753.4:n.27-36928A>C
ENST00000440972.1:c.27-36928A>C ENSP00000406481.1:n.27-36928A>C
NM_181784.2:c.27-36928A>C NP_861449.2:n.27-36928A>C
XM_005264200.3:c.27-36928A>C XP_005264257.2:n.27-36928A>C
XM_005264202.3:c.27-36928A>C XP_005264259.1:n.27-36928A>C
XM_006711966.1:c.27-36928A>C XP_006712029.1:n.27-36928A>C
XM_005264200.5:c.27-36928A>C XP_005264257.2:n.27-36928A>C
XM_005264202.5:c.27-36928A>C XP_005264259.1:n.27-36928A>C
NM_181784.3:c.27-36928A>C MANE Select NP_861449.2:n.27-36928A>C
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