Canonical Allele Identifier: CA151879434
Gene:

Linked Data

dbSNP Id: rs12195036
gnomAD v2: 6-166451697-T-C
gnomAD v3: 6-166038209-T-C
gnomAD v4: 6-166038209-T-C
MyVariant Identifiers: chr6:g.166451697T>C (hg19) chr6:g.166038209T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.166038209T>C , CM000668.2:g.166038209T>C GRCh38
NC_000006.11:g.166451697T>C , CM000668.1:g.166451697T>C GRCh37
NC_000006.10:g.166371687T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943241.1:n.331+1652T>C
XR_943241.2:n.334+1652T>C
Search 100 bp 5'
Search 100 bp 3'