Canonical Allele Identifier: CA598220288
Gene:

Linked Data

dbSNP Id: rs1195002185
gnomAD v2: 11-27757393-T-C
MyVariant Identifiers: chr11:g.27757393T>C (hg19) chr11:g.27735846T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.27735846T>C , CM000673.2:g.27735846T>C GRCh38
NC_000011.9:g.27757393T>C , CM000673.1:g.27757393T>C GRCh37
NC_000011.8:g.27713969T>C NCBI36
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