Canonical Allele Identifier: CA275690881
Gene:

Linked Data

dbSNP Id: rs12437854
gnomAD v2: 15-94141833-T-G
gnomAD v3: 15-93598604-T-G
gnomAD v4: 15-93598604-T-G
MyVariant Identifiers: chr15:g.94141833T>G (hg19) chr15:g.93598604T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.93598604T>G , CM000677.2:g.93598604T>G GRCh38
NC_000015.9:g.94141833T>G , CM000677.1:g.94141833T>G GRCh37
NC_000015.8:g.91942837T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001751681.1:n.1032+5871T>G
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