Canonical Allele Identifier: CA110790427

Gene: AGA

Linked Data

• dbSNP Id: rs978678686
• MyVariant Identifiers: chr4:g.178360970C>G (hg19) ; chr4:g.177439816C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177439816C>G , CM000666.2:g.177439816C>G	GRCh38
NC_000004.11:g.178360970C>G , CM000666.1:g.178360970C>G	GRCh37
NC_000004.10:g.178597964C>G	NCBI36
NG_011845.2:g.7688G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.282-128G>C MANE Select	ENSP00000264595.2:n.282-128G>C
ENST00000264595.6:c.282-128G>C	ENSP00000264595.2:n.282-128G>C
ENST00000506853.5:n.316-128G>C
ENST00000510955.5:n.315+457G>C
NM_000027.3:c.282-128G>C	NP_000018.2:n.282-128G>C
NM_001171988.1:c.282-128G>C	NP_001165459.1:n.282-128G>C
NR_033655.1:n.410-128G>C
XM_006714123.2:c.282-128G>C	XP_006714186.1:n.282-128G>C
XR_001741155.2:n.376-128G>C
NM_000027.4:c.282-128G>C MANE Select	NP_000018.2:n.282-128G>C
NM_001171988.2:c.282-128G>C	NP_001165459.1:n.282-128G>C
NR_033655.2:n.344-128G>C