Canonical Allele Identifier: CA244637525
Gene:

Linked Data

dbSNP Id: rs12321314
gnomAD v2: 12-115836436-G-T
gnomAD v3: 12-115398631-G-T
gnomAD v4: 12-115398631-G-T
MyVariant Identifiers: chr12:g.115836436G>T (hg19) chr12:g.115398631G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.115398631G>T , CM000674.2:g.115398631G>T GRCh38
NC_000012.11:g.115836436G>T , CM000674.1:g.115836436G>T GRCh37
NC_000012.10:g.114320819G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945389.1:n.697+8464C>A
XR_945389.2:n.701+8464C>A
Search 100 bp 5'
Search 100 bp 3'