Canonical Allele Identifier: CA110791461

Gene: AGA

Linked Data

• dbSNP Id: rs956659653
• gnomAD v3: 4-177441851-A-C
• gnomAD v4: 4-177441851-A-C
• MyVariant Identifiers: chr4:g.178363005A>C (hg19) ; chr4:g.177441851A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177441851A>C , CM000666.2:g.177441851A>C	GRCh38
NC_000004.11:g.178363005A>C , CM000666.1:g.178363005A>C	GRCh37
NC_000004.10:g.178599999A>C	NCBI36
NG_011845.2:g.5653T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.127+398T>G MANE Select	ENSP00000264595.2:n.127+398T>G
ENST00000264595.6:c.127+398T>G	ENSP00000264595.2:n.127+398T>G
ENST00000506853.5:n.161+398T>G
ENST00000510955.5:n.161+398T>G
ENST00000511231.1:n.161+398T>G
NM_000027.3:c.127+398T>G	NP_000018.2:n.127+398T>G
NM_001171988.1:c.127+398T>G	NP_001165459.1:n.127+398T>G
NR_033655.1:n.255+398T>G
XM_006714123.2:c.127+398T>G	XP_006714186.1:n.127+398T>G
XR_001741155.2:n.221+398T>G
NM_000027.4:c.127+398T>G MANE Select	NP_000018.2:n.127+398T>G
NM_001171988.2:c.127+398T>G	NP_001165459.1:n.127+398T>G
NR_033655.2:n.189+398T>G