Canonical Allele Identifier: CA13443474
Gene:

Linked Data

dbSNP Id: rs11227306
gnomAD v2: 11-65578672-C-A
gnomAD v3: 11-65811201-C-A
gnomAD v4: 11-65811201-C-A
MyVariant Identifiers: chr11:g.65578672C>A (hg19) chr11:g.65811201C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.65811201C>A , CM000673.2:g.65811201C>A GRCh38
NC_000011.9:g.65578672C>A , CM000673.1:g.65578672C>A GRCh37
NC_000011.8:g.65335248C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011545427.1:c.*1058-7737G>T XP_011543729.1:n.*1058-7737G>T
Search 100 bp 5'
Search 100 bp 3'