Canonical Allele Identifier: CA671767235
Gene:

Linked Data

dbSNP Id: rs1192542003

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112166892G>C , CM000673.2:g.112166892G>C GRCh38
NC_000011.9:g.112037615G>C , CM000673.1:g.112037615G>C GRCh37
NC_000011.8:g.111542825G>C NCBI36
NG_028143.1:g.2226C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000525987.5:n.320-3527G>C
ENST00000531744.5:c.315-3527G>C ENSP00000456957.1:n.315-3527G>C
ENST00000532699.1:c.315-3527G>C ENSP00000456434.1:n.315-3527G>C