Canonical Allele Identifier: CA136859108
Gene:

Linked Data

dbSNP Id: rs116537552
gnomAD v2: 6-31407850-C-T
gnomAD v3: 6-31440073-C-T
gnomAD v4: 6-31440073-C-T
MyVariant Identifiers: chr6:g.31407850C>T (hg19) chr6:g.31440073C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31440073C>T , CM000668.2:g.31440073C>T GRCh38
NC_000006.11:g.31407850C>T , CM000668.1:g.31407850C>T GRCh37
NC_000006.10:g.31515829C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926694.1:n.55-21G>A
Search 100 bp 5'
Search 100 bp 3'