Canonical Allele Identifier: CA139066261

Gene: GCLC

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.53591884T>C , CM000668.2:g.53591884T>C	GRCh38
NC_000006.11:g.53456682T>C , CM000668.1:g.53456682T>C	GRCh37
NC_000006.10:g.53564641T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505197.1:c.-454+25002A>G	ENSP00000427403.1:n.-454+25002A>G