Canonical Allele Identifier: CA556485515

Gene: AGA

Linked Data

• dbSNP Id: rs755452484
• gnomAD v2: 4-178363369-G-T
• gnomAD v4: 4-177442215-G-T
• MyVariant Identifiers: chr4:g.178363369G>T (hg19) ; chr4:g.177442215G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177442215G>T , CM000666.2:g.177442215G>T	GRCh38
NC_000004.11:g.178363369G>T , CM000666.1:g.178363369G>T	GRCh37
NC_000004.10:g.178600363G>T	NCBI36
NG_011845.2:g.5289C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.127+34C>A MANE Select	ENSP00000264595.2:n.127+34C>A
ENST00000264595.6:c.127+34C>A	ENSP00000264595.2:n.127+34C>A
ENST00000506853.5:n.161+34C>A
ENST00000510955.5:n.161+34C>A
ENST00000511231.1:n.161+34C>A
NM_000027.3:c.127+34C>A	NP_000018.2:n.127+34C>A
NM_001171988.1:c.127+34C>A	NP_001165459.1:n.127+34C>A
NR_033655.1:n.255+34C>A
XM_006714123.2:c.127+34C>A	XP_006714186.1:n.127+34C>A
XR_001741155.2:n.221+34C>A
NM_000027.4:c.127+34C>A MANE Select	NP_000018.2:n.127+34C>A
NM_001171988.2:c.127+34C>A	NP_001165459.1:n.127+34C>A
NR_033655.2:n.189+34C>A