Canonical Allele Identifier: CA889164941
Gene:

Linked Data

dbSNP Id: rs1205639771
MyVariant Identifiers: chr1:g.149928442C>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149928442C>G , CM000663.2:g.149928442C>G GRCh38
NC_000001.10:g.149900334C>G , CM000663.1:g.149900334C>G GRCh37
NC_000001.9:g.148166958C>G NCBI36
NG_032777.1:g.4811G>C