Canonical Allele Identifier: CA1515641728
Gene: AGA HGNC NCBI

Linked Data

dbSNP Id: rs1736857000

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177437363A>G , CM000666.2:g.177437363A>G GRCh38
NC_000004.11:g.178358517A>G , CM000666.1:g.178358517A>G GRCh37
NC_000004.10:g.178595511A>G NCBI36
NG_011845.2:g.10141T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264595.7:c.622+42T>C MANE Select ENSP00000264595.2:n.622+42T>C
ENST00000264595.6:c.622+42T>C ENSP00000264595.2:n.622+42T>C
ENST00000502310.5:c.277+42T>C ENSP00000423798.1:n.277+42T>C
ENST00000506853.5:n.656+42T>C
ENST00000510635.1:c.318+42T>C
ENST00000510955.5:n.585T>C
NM_000027.3:c.622+42T>C NP_000018.2:n.622+42T>C
NM_001171988.1:c.622+42T>C NP_001165459.1:n.622+42T>C
NR_033655.1:n.750+42T>C
XM_006714123.2:c.622+42T>C XP_006714186.1:n.622+42T>C
XR_001741155.2:n.716+42T>C
NM_000027.4:c.622+42T>C MANE Select NP_000018.2:n.622+42T>C
NM_001171988.2:c.622+42T>C NP_001165459.1:n.622+42T>C
NR_033655.2:n.684+42T>C