Canonical Allele Identifier: CA15847825
Gene:

Linked Data

dbSNP Id: rs10152591
gnomAD v2: 15-70048157-A-C
gnomAD v3: 15-69755818-A-C
gnomAD v4: 15-69755818-A-C
MyVariant Identifiers: chr15:g.70048157A>C (hg19) chr15:g.69755818A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.69755818A>C , CM000677.2:g.69755818A>C GRCh38
NC_000015.9:g.70048157A>C , CM000677.1:g.70048157A>C GRCh37
NC_000015.8:g.67835211A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001751592.2:n.86-338A>C
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