Canonical Allele Identifier: CA542915336

Gene: GNL3

Linked Data

• dbSNP Id: rs1108842
• gnomAD v2: 3-52720080-A-G
• gnomAD v4: 3-52686064-A-G
• MyVariant Identifiers: chr3:g.52720080A>G (hg19) ; chr3:g.52686064A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52686064A>G , CM000665.2:g.52686064A>G	GRCh38
NC_000003.11:g.52720080A>G , CM000665.1:g.52720080A>G	GRCh37
NC_000003.10:g.52695120A>G	NCBI36
NG_027871.1:g.5145A>G
NG_032108.1:g.4787T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000418458.6:c.-29A>G MANE Select	ENSP00000395772.1:n.-29A>G
ENST00000394799.6:c.-162A>G	ENSP00000378278.2:n.-162A>G
ENST00000418458.5:c.-29A>G	ENSP00000395772.1:n.-29A>G
ENST00000462550.5:n.33A>G
ENST00000468146.5:n.60A>G
ENST00000468885.1:n.35A>G
ENST00000479230.5:c.-23-705A>G	ENSP00000419734.1:n.-23-705A>G
ENST00000492349.5:c.-29A>G	ENSP00000420345.1:n.-29A>G
ENST00000496254.5:n.16A>G
NM_014366.4:c.-29A>G	NP_055181.3:n.-29A>G
NM_206825.1:c.-162A>G	NP_996561.1:n.-162A>G
NM_206826.1:c.-24+9A>G	NP_996562.1:n.-24+9A>G
NM_014366.5:c.-29A>G MANE Select	NP_055181.3:n.-29A>G
NM_206825.2:c.-162A>G	NP_996561.1:n.-162A>G