Canonical Allele Identifier: CA136858869
Gene:

Linked Data

dbSNP Id: rs745493276
gnomAD v3: 6-31439645-C-T
gnomAD v4: 6-31439645-C-T
MyVariant Identifiers: chr6:g.31407422C>T (hg19) chr6:g.31439645C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31439645C>T , CM000668.2:g.31439645C>T GRCh38
NC_000006.11:g.31407422C>T , CM000668.1:g.31407422C>T GRCh37
NC_000006.10:g.31515401C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926694.1:n.462G>A
Search 100 bp 5'
Search 100 bp 3'