Canonical Allele Identifier: CA473651113

Gene:

Linked Data

• gnomAD v4: 11-27484085-G-C
• MyVariant Identifiers: chr11:g.27505632G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.27484085G>C , CM000673.2:g.27484085G>C	GRCh38
NC_000011.9:g.27505632G>C , CM000673.1:g.27505632G>C	GRCh37
NC_000011.8:g.27462208G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496450.1:n.236G>C