Canonical Allele Identifier: CA3146907

Gene: AGA

Linked Data

• dbSNP Id: rs766165178
• ExAC: 4:178359897 A / G
• gnomAD v2: 4-178359897-A-G
• gnomAD v4: 4-177438743-A-G
• MyVariant Identifiers: chr4:g.178359897A>G (hg19) ; chr4:g.177438743A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177438743A>G , CM000666.2:g.177438743A>G	GRCh38
NC_000004.11:g.178359897A>G , CM000666.1:g.178359897A>G	GRCh37
NC_000004.10:g.178596891A>G	NCBI36
NG_011845.2:g.8761T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.507+2T>C MANE Select	ENSP00000264595.2:n.507+2T>C
ENST00000264595.6:c.507+2T>C	ENSP00000264595.2:n.507+2T>C
ENST00000502310.5:c.162+2T>C	ENSP00000423798.1:n.162+2T>C
ENST00000506853.5:n.541+2T>C
ENST00000510635.1:c.203+2T>C
ENST00000510955.5:n.428+2T>C
NM_000027.3:c.507+2T>C	NP_000018.2:n.507+2T>C
NM_001171988.1:c.507+2T>C	NP_001165459.1:n.507+2T>C
NR_033655.1:n.635+2T>C
XM_006714123.2:c.507+2T>C	XP_006714186.1:n.507+2T>C
XR_001741155.2:n.601+2T>C
NM_000027.4:c.507+2T>C MANE Select	NP_000018.2:n.507+2T>C
NM_001171988.2:c.507+2T>C	NP_001165459.1:n.507+2T>C
NR_033655.2:n.569+2T>C