Canonical Allele Identifier: CA151235268
Gene:

Linked Data

dbSNP Id: rs999696686
gnomAD v3: 6-160668477-C-T
gnomAD v4: 6-160668477-C-T
MyVariant Identifiers: chr6:g.161089509C>T (hg19) chr6:g.160668477C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160668477C>T , CM000668.2:g.160668477C>T GRCh38
NC_000006.11:g.161089509C>T , CM000668.1:g.161089509C>T GRCh37
NC_000006.10:g.161009499C>T NCBI36
NG_016147.1:g.2899G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000452651.1:n.115-2104G>A
Search 100 bp 5'
Search 100 bp 3'