Canonical Allele Identifier: CA816711679
Gene:

Linked Data

dbSNP Id: rs1377919363
gnomAD v3: 6-105805175-A-G
gnomAD v4: 6-105805175-A-G
MyVariant Identifiers: chr6:g.106253050A>G (hg19) chr6:g.105805175A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.105805175A>G , CM000668.2:g.105805175A>G GRCh38
NC_000006.11:g.106253050A>G , CM000668.1:g.106253050A>G GRCh37
NC_000006.10:g.106359743A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_942835.1:n.510+24882T>C
XR_001744274.1:n.438+24882T>C
XR_001744275.1:n.337+24882T>C
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