Canonical Allele Identifier: CA2672748587
Gene: AGA HGNC NCBI

Linked Data

gnomAD v4: 4-177442412-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177442412C>T , CM000666.2:g.177442412C>T GRCh38
NC_000004.11:g.178363566C>T , CM000666.1:g.178363566C>T GRCh37
NC_000004.10:g.178600560C>T NCBI36
NG_011845.2:g.5092G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264595.7:c.-37G>A MANE Select ENSP00000264595.2:n.-37G>A
ENST00000264595.6:c.-37G>A ENSP00000264595.2:n.-37G>A
NM_000027.3:c.-37G>A NP_000018.2:n.-37G>A
NM_001171988.1:c.-37G>A NP_001165459.1:n.-37G>A
NR_033655.1:n.92G>A
XM_006714123.2:c.-37G>A XP_006714186.1:n.-37G>A
XR_001741155.2:n.58G>A
NM_000027.4:c.-37G>A MANE Select NP_000018.2:n.-37G>A
NM_001171988.2:c.-37G>A NP_001165459.1:n.-37G>A
NR_033655.2:n.26G>A
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