Canonical Allele Identifier: CA10907788
Gene:

Linked Data

dbSNP Id: rs10788819
gnomAD v2: 1-151895093-C-T
gnomAD v3: 1-151922617-C-T
gnomAD v4: 1-151922617-C-T
MyVariant Identifiers: chr1:g.151895093C>T (hg19) chr1:g.151922617C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.151922617C>T , CM000663.2:g.151922617C>T GRCh38
NC_000001.10:g.151895093C>T , CM000663.1:g.151895093C>T GRCh37
NC_000001.9:g.150161717C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_922139.1:n.163-65G>A
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