Canonical Allele Identifier: CA10788357

Linked Data

dbSNP Id: rs2222202

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206772036G>A , CM000663.2:g.206772036G>A GRCh38
NC_000001.10:g.206945381G>A , CM000663.1:g.206945381G>A GRCh37
NC_000001.9:g.205012004G>A NCBI36
NG_012088.1:g.5459C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000656872.2:c.-149+1206G>A ENSP00000499487.2:p.=
ENST00000659065.1:c.48+235C>T ENSP00000499588.1:p.=
ENST00000659642.1:c.48+235C>T ENSP00000499509.1:p.=
ENST00000659997.2:c.-149+958G>A ENSP00000499459.2:p.=
ENST00000662320.1:n.67+1206G>A
ENST00000664374.1:c.48+235C>T ENSP00000499664.1:p.=
ENST00000423557.1:c.165+235C>T (IL10) MANE Select ENSP00000412237.1:p.=
NM_000572.2:c.165+235C>T (IL10) NP_000563.1:p.=
XM_011509506.1:c.165+235C>T (IL10) XP_011507808.1:p.=
NM_000572.3:c.165+235C>T (IL10) MANE Select NP_000563.1:p.=
NM_153758.3:c.-35+958G>A (IL19) NP_715639.1:p.=
NM_001393490.1:c.-149+1206G>A (IL19) NP_001380419.1:p.=
NM_153758.5:c.-149+958G>A (IL19) NP_715639.2:p.=
NR_168466.1:n.224+235C>T (IL10)