Canonical Allele Identifier: CA846669363
Gene:

Linked Data

dbSNP Id: rs181790342
gnomAD v3: 8-122396242-G-T
gnomAD v4: 8-122396242-G-T
MyVariant Identifiers: chr8:g.123408481G>T (hg19) chr8:g.122396242G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.122396242G>T , CM000670.2:g.122396242G>T GRCh38
NC_000008.10:g.123408481G>T , CM000670.1:g.123408481G>T GRCh37
NC_000008.9:g.123477662G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928599.1:n.152+2930C>A
XR_928599.3:n.152+2930C>A
Search 100 bp 5'
Search 100 bp 3'