Canonical Allele Identifier: CA2456080
Gene: IL17RB HGNC NCBI
ClinVar RCV:
ClinVar Variation:
MyVariant.info:
Revel Score:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.53849742C>G , CM000665.2:g.53849742C>G GRCh38
NC_000003.11:g.53883769C>G , CM000665.1:g.53883769C>G GRCh37
NC_000003.10:g.53858809C>G NCBI36
NG_028042.1:g.1652G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000288167.8:c.173C>G MANE Select ENSP00000288167.3:p.Ala58Gly
ENST00000288167.7:c.173C>G ENSP00000288167.3:p.Ala58Gly
ENST00000475124.1:n.178C>G
ENST00000494338.1:c.173C>G ENSP00000418638.1:p.Ala58Gly
NM_018725.3:c.173C>G NP_061195.2:p.Ala58Gly
XM_005265310.3:c.173C>G XP_005265367.1:p.Ala58Gly
XM_005265311.3:c.173C>G XP_005265368.1:p.Ala58Gly
XM_005265312.3:c.173C>G XP_005265369.1:p.Ala58Gly
XM_011533940.1:c.-51C>G XP_011532242.1:n.-51C>G
XM_011533941.1:c.173C>G XP_011532243.1:p.Ala58Gly
XR_245147.3:n.212C>G
XR_940467.1:n.212C>G
XR_940468.1:n.212C>G
XM_005265310.5:c.173C>G XP_005265367.1:p.Ala58Gly
XM_005265311.5:c.173C>G XP_005265368.1:p.Ala58Gly
XM_005265312.5:c.173C>G XP_005265369.1:p.Ala58Gly
XM_011533941.3:c.173C>G XP_011532243.1:p.Ala58Gly
XM_017006804.2:c.-51C>G XP_016862293.1:n.-51C>G
XM_017006805.2:c.-51C>G XP_016862294.1:n.-51C>G
XM_017006806.2:c.-51C>G XP_016862295.1:n.-51C>G
XM_017006807.2:c.173C>G XP_016862296.1:p.Ala58Gly
XM_024453634.1:c.173C>G XP_024309402.1:p.Ala58Gly
XM_024453635.1:c.173C>G XP_024309403.1:p.Ala58Gly
XM_024453636.1:c.173C>G XP_024309404.1:p.Ala58Gly
NM_018725.4:c.173C>G MANE Select NP_061195.2:p.Ala58Gly