Canonical Allele Identifier: CA473651196
Gene:

Linked Data

dbSNP Id: rs1865049916
gnomAD v3: 11-27484114-T-A
gnomAD v4: 11-27484114-T-A
MyVariant Identifiers: chr11:g.27505661T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.27484114T>A , CM000673.2:g.27484114T>A GRCh38
NC_000011.9:g.27505661T>A , CM000673.1:g.27505661T>A GRCh37
NC_000011.8:g.27462237T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000496450.1:n.265T>A
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