Canonical Allele Identifier: CA558995700

Gene: IL7R

Linked Data

• dbSNP Id: rs1177613188
• gnomAD v2: 5-35867715-A-G
• gnomAD v4: 5-35867613-A-G
• MyVariant Identifiers: chr5:g.35867715A>G (hg19) ; chr5:g.35867613A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35867613A>G , CM000667.2:g.35867613A>G	GRCh38
NC_000005.9:g.35867715A>G , CM000667.1:g.35867715A>G	GRCh37
NC_000005.8:g.35903472A>G	NCBI36
NG_009567.1:g.15725A>G , LRG_74:g.15725A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303115.8:c.379+150A>G MANE Select	ENSP00000306157.3:n.379+150A>G
ENST00000303115.7:c.379+150A>G	ENSP00000306157.3:n.379+150A>G
ENST00000506850.5:c.379+150A>G	ENSP00000421207.1:n.379+150A>G
ENST00000514217.5:c.379+150A>G	ENSP00000427688.1:n.379+150A>G
NM_002185.3:c.379+150A>G	NP_002176.2:n.379+150A>G
NR_120485.1:n.482+150A>G
XM_005248299.2:c.379+150A>G	XP_005248356.1:n.379+150A>G
XM_005248300.1:c.379+150A>G	XP_005248357.1:n.379+150A>G
XM_011514037.1:c.379+150A>G	XP_011512339.1:n.379+150A>G
NM_002185.4:c.379+150A>G	NP_002176.2:n.379+150A>G
NR_120485.2:n.508+150A>G
XM_005248299.4:c.379+150A>G	XP_005248356.1:n.379+150A>G
NM_002185.5:c.379+150A>G MANE Select	NP_002176.2:n.379+150A>G
NR_120485.3:n.466+150A>G