Canonical Allele Identifier: CA10699328

Gene: IL24

Linked Data

• dbSNP Id: rs1150256
• gnomAD v2: 1-207073133-G-A
• gnomAD v3: 1-206899788-G-A
• gnomAD v4: 1-206899788-G-A
• MyVariant Identifiers: chr1:g.207073133G>A (hg19) ; chr1:g.206899788G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206899788G>A , CM000663.2:g.206899788G>A	GRCh38
NC_000001.10:g.207073133G>A , CM000663.1:g.207073133G>A	GRCh37
NC_000001.9:g.205139756G>A	NCBI36
NG_029565.1:g.7346G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000294984.7:c.240+273G>A MANE Select	ENSP00000294984.2:n.240+273G>A
ENST00000294984.6:c.240+273G>A	ENSP00000294984.2:n.240+273G>A
ENST00000367093.3:c.243+273G>A	ENSP00000356060.3:n.243+273G>A
ENST00000367095.7:c.45-507G>A	ENSP00000356062.3:n.45-507G>A
ENST00000391929.7:c.243+273G>A	ENSP00000375795.3:n.243+273G>A
ENST00000480741.1:c.45-507G>A	ENSP00000418933.1:n.45-507G>A
ENST00000491169.1:n.152-507G>A
ENST00000611909.4:c.45-507G>A	ENSP00000484900.1:n.45-507G>A
NM_001185156.1:c.243+273G>A	NP_001172085.1:n.243+273G>A
NM_001185157.1:c.243+273G>A	NP_001172086.1:n.243+273G>A
NM_001185158.1:c.45-507G>A	NP_001172087.1:n.45-507G>A
NM_006850.3:c.240+273G>A MANE Select	NP_006841.1:n.240+273G>A
XM_011509101.1:c.159+273G>A	XP_011507403.1:n.159+273G>A
XM_011509101.2:c.159+273G>A	XP_011507403.1:n.159+273G>A
XM_017000121.1:c.159+273G>A	XP_016855610.1:n.159+273G>A