Canonical Allele Identifier: CA185200461
Gene:

Linked Data

dbSNP Id: rs1015271710
gnomAD v2: 8-123408520-A-T
gnomAD v3: 8-122396281-A-T
gnomAD v4: 8-122396281-A-T
MyVariant Identifiers: chr8:g.123408520A>T (hg19) chr8:g.122396281A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.122396281A>T , CM000670.2:g.122396281A>T GRCh38
NC_000008.10:g.123408520A>T , CM000670.1:g.123408520A>T GRCh37
NC_000008.9:g.123477701A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928599.1:n.152+2891T>A
XR_928599.3:n.152+2891T>A
Search 100 bp 5'
Search 100 bp 3'