Canonical Allele Identifier: CA185200466
Gene:

Linked Data

dbSNP Id: rs779138548
gnomAD v2: 8-123408565-G-A
gnomAD v3: 8-122396326-G-A
gnomAD v4: 8-122396326-G-A
MyVariant Identifiers: chr8:g.123408565G>A (hg19) chr8:g.122396326G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.122396326G>A , CM000670.2:g.122396326G>A GRCh38
NC_000008.10:g.123408565G>A , CM000670.1:g.123408565G>A GRCh37
NC_000008.9:g.123477746G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928599.1:n.152+2846C>T
XR_928599.3:n.152+2846C>T
Search 100 bp 5'
Search 100 bp 3'