Canonical Allele Identifier: CA224070817
Gene:

Linked Data

dbSNP Id: rs926919802
gnomAD v2: 11-66278041-C-T
gnomAD v3: 11-66510570-C-T
gnomAD v4: 11-66510570-C-T
MyVariant Identifiers: chr11:g.66278041C>T (hg19) chr11:g.66510570C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66510570C>T , CM000673.2:g.66510570C>T GRCh38
NC_000011.9:g.66278041C>T , CM000673.1:g.66278041C>T GRCh37
NC_000011.8:g.66034617C>T NCBI36
NG_009093.1:g.4923C>T
NG_032068.1:g.35162C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000419755.3:c.159-443C>T ENSP00000398526.3:n.159-443C>T
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