Canonical Allele Identifier: CA151235368
Gene:

Linked Data

dbSNP Id: rs909666148
gnomAD v3: 6-160668558-C-T
gnomAD v4: 6-160668558-C-T
MyVariant Identifiers: chr6:g.161089590C>T (hg19) chr6:g.160668558C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160668558C>T , CM000668.2:g.160668558C>T GRCh38
NC_000006.11:g.161089590C>T , CM000668.1:g.161089590C>T GRCh37
NC_000006.10:g.161009580C>T NCBI36
NG_016147.1:g.2818G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000452651.1:n.115-2185G>A
Search 100 bp 5'
Search 100 bp 3'