Canonical Allele Identifier: CA10699287

Linked Data

dbSNP Id: rs3021094

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206771607T>G , CM000663.2:g.206771607T>G GRCh38
NC_000001.10:g.206944952T>G , CM000663.1:g.206944952T>G GRCh37
NC_000001.9:g.205011575T>G NCBI36
NG_012088.1:g.5888A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000656872.2:c.-149+777T>G ENSP00000499487.2:p.=
ENST00000659065.1:c.49-192A>C ENSP00000499588.1:p.=
ENST00000659642.1:c.49-192A>C ENSP00000499509.1:p.=
ENST00000659997.2:c.-149+529T>G ENSP00000499459.2:p.=
ENST00000662320.1:n.67+777T>G
ENST00000664374.1:c.49-192A>C ENSP00000499664.1:p.=
ENST00000423557.1:c.166-192A>C (IL10) MANE Select ENSP00000412237.1:p.=
NM_000572.2:c.166-192A>C (IL10) NP_000563.1:p.=
XM_011509506.1:c.166-192A>C (IL10) XP_011507808.1:p.=
NM_000572.3:c.166-192A>C (IL10) MANE Select NP_000563.1:p.=
NM_153758.3:c.-35+529T>G (IL19) NP_715639.1:p.=
NM_001393490.1:c.-149+777T>G (IL19) NP_001380419.1:p.=
NM_153758.5:c.-149+529T>G (IL19) NP_715639.2:p.=
NR_168466.1:n.225-192A>C (IL10)