Canonical Allele Identifier: CA1363760

Linked Data

dbSNP Id: rs1554286

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206770888A>G , CM000663.2:g.206770888A>G GRCh38
NC_000001.10:g.206944233A>G , CM000663.1:g.206944233A>G GRCh37
NC_000001.9:g.205010856A>G NCBI36
NG_012088.1:g.6607T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000656872.2:c.-149+58A>G ENSP00000499487.2:p.=
ENST00000659065.1:c.261+19T>C ENSP00000499588.1:p.=
ENST00000659642.1:c.261+19T>C ENSP00000499509.1:p.=
ENST00000659997.2:c.-339A>G ENSP00000499459.2:p.=
ENST00000662320.1:n.67+58A>G
ENST00000664374.1:c.261+19T>C ENSP00000499664.1:p.=
ENST00000367099.3:n.283+19T>C
ENST00000423557.1:c.378+19T>C (IL10) MANE Select ENSP00000412237.1:p.=
ENST00000471071.1:n.293+19T>C
NM_000572.2:c.378+19T>C (IL10) NP_000563.1:p.=
XM_011509506.1:c.378+19T>C (IL10) XP_011507808.1:p.=
NM_000572.3:c.378+19T>C (IL10) MANE Select NP_000563.1:p.=
NM_153758.3:c.-225A>G (IL19) NP_715639.1:p.=
NM_001382624.1:c.123+19T>C (IL10) NP_001369553.1:p.=
NM_001393490.1:c.-149+58A>G (IL19) NP_001380419.1:p.=
NM_153758.5:c.-339A>G (IL19) NP_715639.2:p.=
NR_168466.1:n.437+19T>C (IL10)