Canonical Allele Identifier: CA1638480432
Gene:

Linked Data

dbSNP Id: rs6912405

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.74161515A>C , CM000668.2:g.74161515A>C GRCh38
NC_000006.11:g.74871231A>C , CM000668.1:g.74871231A>C GRCh37
NC_000006.10:g.74927951A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110856.1:n.138+91927A>C