Canonical Allele Identifier: CA139062444
Gene: GCLC HGNC NCBI

Linked Data

dbSNP Id: rs963613181
MyVariant Identifiers: chr6:g.53410121T>G (hg19) chr6:g.53545323T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.53545323T>G , CM000668.2:g.53545323T>G GRCh38
NC_000006.11:g.53410121T>G , CM000668.1:g.53410121T>G GRCh37
NC_000006.10:g.53518080T>G NCBI36
NG_012071.1:g.4711A>C
NG_012071.2:g.4807A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000616923.5:c.-10+2733A>C ENSP00000482756.2:n.-10+2733A>C
ENST00000505197.1:c.-10+18794A>C ENSP00000427403.1:n.-10+18794A>C
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