Canonical Allele Identifier: CA145511531
Gene:

Linked Data

dbSNP Id: rs145313966
gnomAD v3: 6-105805154-A-C
gnomAD v4: 6-105805154-A-C
MyVariant Identifiers: chr6:g.106253029A>C (hg19) chr6:g.105805154A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.105805154A>C , CM000668.2:g.105805154A>C GRCh38
NC_000006.11:g.106253029A>C , CM000668.1:g.106253029A>C GRCh37
NC_000006.10:g.106359722A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_942835.1:n.510+24903T>G
XR_001744274.1:n.438+24903T>G
XR_001744275.1:n.337+24903T>G
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