Canonical Allele Identifier: CA224070841
Gene:

Linked Data

dbSNP Id: rs544467266
gnomAD v4: 11-66510587-C-T
MyVariant Identifiers: chr11:g.66278058C>T (hg19) chr11:g.66510587C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66510587C>T , CM000673.2:g.66510587C>T GRCh38
NC_000011.9:g.66278058C>T , CM000673.1:g.66278058C>T GRCh37
NC_000011.8:g.66034634C>T NCBI36
NG_009093.1:g.4940C>T
NG_032068.1:g.35179C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000419755.3:c.159-426C>T ENSP00000398526.3:n.159-426C>T
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