Canonical Allele Identifier: CA3146887

Gene: AGA

Linked Data

• dbSNP Id: rs749950004
• ExAC: 4:178358598 G / C
• gnomAD v4: 4-177437444-G-C
• MyVariant Identifiers: chr4:g.178358598G>C (hg19) ; chr4:g.177437444G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177437444G>C , CM000666.2:g.177437444G>C	GRCh38
NC_000004.11:g.178358598G>C , CM000666.1:g.178358598G>C	GRCh37
NC_000004.10:g.178595592G>C	NCBI36
NG_011845.2:g.10060C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.583C>G MANE Select	ENSP00000264595.2:p.His195Asp
ENST00000264595.6:c.583C>G	ENSP00000264595.2:p.His195Asp
ENST00000502310.5:c.238C>G	ENSP00000423798.1:p.His80Asp
ENST00000506853.5:n.617C>G
ENST00000510635.1:c.279C>G
ENST00000510955.5:n.504C>G
NM_000027.3:c.583C>G	NP_000018.2:p.His195Asp
NM_001171988.1:c.583C>G	NP_001165459.1:p.His195Asp
NR_033655.1:n.711C>G
XM_006714123.2:c.583C>G	XP_006714186.1:p.His195Asp
XR_001741155.2:n.677C>G
NM_000027.4:c.583C>G MANE Select	NP_000018.2:p.His195Asp
NM_001171988.2:c.583C>G	NP_001165459.1:p.His195Asp
NR_033655.2:n.645C>G