Canonical Allele Identifier: CA791503397

Gene: AGA

Linked Data

• dbSNP Id: rs1024786776
• gnomAD v3: 4-177442091-C-G
• gnomAD v4: 4-177442091-C-G
• MyVariant Identifiers: chr4:g.178363245C>G (hg19) ; chr4:g.177442091C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177442091C>G , CM000666.2:g.177442091C>G	GRCh38
NC_000004.11:g.178363245C>G , CM000666.1:g.178363245C>G	GRCh37
NC_000004.10:g.178600239C>G	NCBI36
NG_011845.2:g.5413G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000264595.7:c.127+158G>C MANE Select	ENSP00000264595.2:n.127+158G>C
ENST00000264595.6:c.127+158G>C	ENSP00000264595.2:n.127+158G>C
ENST00000506853.5:n.161+158G>C
ENST00000510955.5:n.161+158G>C
ENST00000511231.1:n.161+158G>C
NM_000027.3:c.127+158G>C	NP_000018.2:n.127+158G>C
NM_001171988.1:c.127+158G>C	NP_001165459.1:n.127+158G>C
NR_033655.1:n.255+158G>C
XM_006714123.2:c.127+158G>C	XP_006714186.1:n.127+158G>C
XR_001741155.2:n.221+158G>C
NM_000027.4:c.127+158G>C MANE Select	NP_000018.2:n.127+158G>C
NM_001171988.2:c.127+158G>C	NP_001165459.1:n.127+158G>C
NR_033655.2:n.189+158G>C