Canonical Allele Identifier: CA966229

Gene: AGL

Linked Data

• dbSNP Id: rs780324261
• ExAC: 1:100335911 C / G
• gnomAD v2: 1-100335911-C-G
• gnomAD v4: 1-99870355-C-G
• MyVariant Identifiers: chr1:g.100335911C>G (hg19) ; chr1:g.99870355C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99870355C>G , CM000663.2:g.99870355C>G	GRCh38
NC_000001.10:g.100335911C>G , CM000663.1:g.100335911C>G	GRCh37
NC_000001.9:g.100108499C>G	NCBI36
NG_012865.1:g.25272C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.665-45C>G MANE Select	ENSP00000355106.3:n.665-45C>G
ENST00000637337.1:n.876-45C>G
ENST00000294724.8:c.665-45C>G	ENSP00000294724.4:n.665-45C>G
ENST00000361302.7:c.617-45C>G	ENSP00000354971.3:n.617-45C>G
ENST00000361522.4:c.614-45C>G	ENSP00000354635.4:n.614-45C>G
ENST00000361915.7:c.665-45C>G	ENSP00000355106.3:n.665-45C>G
ENST00000370161.6:c.617-45C>G	ENSP00000359180.2:n.617-45C>G
ENST00000370163.7:c.665-45C>G	ENSP00000359182.3:n.665-45C>G
ENST00000370165.7:c.665-45C>G	ENSP00000359184.3:n.665-45C>G
NM_000028.2:c.665-45C>G	NP_000019.2:n.665-45C>G
NM_000642.2:c.665-45C>G	NP_000633.2:n.665-45C>G
NM_000643.2:c.665-45C>G	NP_000634.2:n.665-45C>G
NM_000644.2:c.665-45C>G	NP_000635.2:n.665-45C>G
NM_000645.2:c.614-45C>G	NP_000636.2:n.614-45C>G
NM_000646.2:c.617-45C>G	NP_000637.2:n.617-45C>G
XM_005270557.1:c.665-45C>G	XP_005270614.1:n.665-45C>G
XM_005270557.2:c.665-45C>G	XP_005270614.1:n.665-45C>G
NM_000642.3:c.665-45C>G MANE Select	NP_000633.2:n.665-45C>G