Canonical Allele Identifier: CA1515642078
Gene: AGA HGNC NCBI

Linked Data

dbSNP Id: rs1736865361

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177437559T>A , CM000666.2:g.177437559T>A GRCh38
NC_000004.11:g.178358713T>A , CM000666.1:g.178358713T>A GRCh37
NC_000004.10:g.178595707T>A NCBI36
NG_011845.2:g.9945A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264595.7:c.508-40A>T MANE Select ENSP00000264595.2:n.508-40A>T
ENST00000264595.6:c.508-40A>T ENSP00000264595.2:n.508-40A>T
ENST00000502310.5:c.163-40A>T ENSP00000423798.1:n.163-40A>T
ENST00000506853.5:n.542-40A>T
ENST00000510635.1:c.204-40A>T
ENST00000510955.5:n.429-40A>T
NM_000027.3:c.508-40A>T NP_000018.2:n.508-40A>T
NM_001171988.1:c.508-40A>T NP_001165459.1:n.508-40A>T
NR_033655.1:n.636-40A>T
XM_006714123.2:c.508-40A>T XP_006714186.1:n.508-40A>T
XR_001741155.2:n.602-40A>T
NM_000027.4:c.508-40A>T MANE Select NP_000018.2:n.508-40A>T
NM_001171988.2:c.508-40A>T NP_001165459.1:n.508-40A>T
NR_033655.2:n.570-40A>T