Canonical Allele Identifier: CA110790415

Gene: AGA

Linked Data

• dbSNP Id: rs967264121
• gnomAD v2: 4-178360960-G-A
• gnomAD v3: 4-177439806-G-A
• gnomAD v4: 4-177439806-G-A
• MyVariant Identifiers: chr4:g.178360960G>A (hg19) ; chr4:g.177439806G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177439806G>A , CM000666.2:g.177439806G>A	GRCh38
NC_000004.11:g.178360960G>A , CM000666.1:g.178360960G>A	GRCh37
NC_000004.10:g.178597954G>A	NCBI36
NG_011845.2:g.7698C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.282-118C>T MANE Select	ENSP00000264595.2:n.282-118C>T
ENST00000264595.6:c.282-118C>T	ENSP00000264595.2:n.282-118C>T
ENST00000506853.5:n.316-118C>T
ENST00000510955.5:n.315+467C>T
NM_000027.3:c.282-118C>T	NP_000018.2:n.282-118C>T
NM_001171988.1:c.282-118C>T	NP_001165459.1:n.282-118C>T
NR_033655.1:n.410-118C>T
XM_006714123.2:c.282-118C>T	XP_006714186.1:n.282-118C>T
XR_001741155.2:n.376-118C>T
NM_000027.4:c.282-118C>T MANE Select	NP_000018.2:n.282-118C>T
NM_001171988.2:c.282-118C>T	NP_001165459.1:n.282-118C>T
NR_033655.2:n.344-118C>T