Canonical Allele Identifier: CA1629330156
Gene: GCLC HGNC NCBI

Linked Data

dbSNP Id: rs1763438215

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.53545305T>C , CM000668.2:g.53545305T>C GRCh38
NC_000006.11:g.53410103T>C , CM000668.1:g.53410103T>C GRCh37
NC_000006.10:g.53518062T>C NCBI36
NG_012071.1:g.4729A>G
NG_012071.2:g.4825A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000616923.5:c.-10+2751A>G ENSP00000482756.2:n.-10+2751A>G
ENST00000505197.1:c.-10+18812A>G ENSP00000427403.1:n.-10+18812A>G