Canonical Allele Identifier: CA3146966

Gene: AGA

Linked Data

• dbSNP Id: rs769155621
• ExAC: 4:178360889 T / C
• gnomAD v2: 4-178360889-T-C
• gnomAD v3: 4-177439735-T-C
• gnomAD v4: 4-177439735-T-C
• MyVariant Identifiers: chr4:g.178360889T>C (hg19) ; chr4:g.177439735T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177439735T>C , CM000666.2:g.177439735T>C	GRCh38
NC_000004.11:g.178360889T>C , CM000666.1:g.178360889T>C	GRCh37
NC_000004.10:g.178597883T>C	NCBI36
NG_011845.2:g.7769A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.282-47A>G MANE Select	ENSP00000264595.2:n.282-47A>G
ENST00000264595.6:c.282-47A>G	ENSP00000264595.2:n.282-47A>G
ENST00000506853.5:n.316-47A>G
ENST00000510955.5:n.315+538A>G
NM_000027.3:c.282-47A>G	NP_000018.2:n.282-47A>G
NM_001171988.1:c.282-47A>G	NP_001165459.1:n.282-47A>G
NR_033655.1:n.410-47A>G
XM_006714123.2:c.282-47A>G	XP_006714186.1:n.282-47A>G
XR_001741155.2:n.376-47A>G
NM_000027.4:c.282-47A>G MANE Select	NP_000018.2:n.282-47A>G
NM_001171988.2:c.282-47A>G	NP_001165459.1:n.282-47A>G
NR_033655.2:n.344-47A>G