Canonical Allele Identifier: CA150162988
Gene:

Identifiers and link-outs to other resources

dbSNP Id: rs140068132

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151633699A>G , CM000668.2:g.151633699A>G GRCh38
NC_000006.11:g.151954834A>G , CM000668.1:g.151954834A>G GRCh37
NC_000006.10:g.151996527A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943115.1:n.2496+3717A>G