Canonical Allele Identifier: CA1629330136
Gene: GCLC HGNC NCBI

Linked Data

dbSNP Id: rs1763436834
gnomAD v4: 6-53545263-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.53545263G>T , CM000668.2:g.53545263G>T GRCh38
NC_000006.11:g.53410061G>T , CM000668.1:g.53410061G>T GRCh37
NC_000006.10:g.53518020G>T NCBI36
NG_012071.1:g.4771C>A
NG_012071.2:g.4867C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000616923.5:c.-10+2793C>A ENSP00000482756.2:n.-10+2793C>A
ENST00000505197.1:c.-10+18854C>A ENSP00000427403.1:n.-10+18854C>A