Canonical Allele Identifier: CA347946679

Gene: IL18RAP

Linked Data

• gnomAD v4: 2-102451811-G-T
• MyVariant Identifiers: chr2:g.103068271G>T (hg19) ; chr2:g.102451811G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.102451811G>T , CM000664.2:g.102451811G>T	GRCh38
NC_000002.11:g.103068271G>T , CM000664.1:g.103068271G>T	GRCh37
NC_000002.10:g.102434703G>T	NCBI36
NG_011481.1:g.38018G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000687160.1:c.1430G>T MANE Select	ENSP00000510345.1:p.Gly477Val
ENST00000264260.6:c.1430G>T	ENSP00000264260.2:p.Gly477Val
ENST00000409369.1:c.1004G>T	ENSP00000387201.1:p.Gly335Val
NM_003853.3:c.1430G>T	NP_003844.1:p.Gly477Val
XM_011512087.1:c.1004G>T	XP_011510389.1:p.Gly335Val
XM_011512088.1:c.1004G>T	XP_011510390.1:p.Gly335Val
XM_011512087.2:c.1004G>T	XP_011510389.1:p.Gly335Val
XM_011512088.2:c.1004G>T	XP_011510390.1:p.Gly335Val
XM_017005173.1:c.572G>T	XP_016860662.1:p.Gly191Val
XM_024453197.1:c.1430G>T	XP_024308965.1:p.Gly477Val
XM_024453198.1:c.1430G>T	XP_024308966.1:p.Gly477Val
XM_024453199.1:c.1430G>T	XP_024308967.1:p.Gly477Val
XM_024453200.1:c.1430G>T	XP_024308968.1:p.Gly477Val
XM_024453201.1:c.1430G>T	XP_024308969.1:p.Gly477Val
NM_001393486.1:c.1430G>T	NP_001380415.1:p.Gly477Val
NM_001393487.1:c.1430G>T MANE Select	NP_001380416.1:p.Gly477Val
NM_001393488.1:c.1004G>T	NP_001380417.1:p.Gly335Val
NM_001393489.1:c.1004G>T	NP_001380418.1:p.Gly335Val
NM_003853.4:c.1430G>T	NP_003844.1:p.Gly477Val