Canonical Allele Identifier: CA816711660
Gene:

Linked Data

dbSNP Id: rs1325622763
gnomAD v3: 6-105805147-G-C
gnomAD v4: 6-105805147-G-C
MyVariant Identifiers: chr6:g.106253022G>C (hg19) chr6:g.105805147G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.105805147G>C , CM000668.2:g.105805147G>C GRCh38
NC_000006.11:g.106253022G>C , CM000668.1:g.106253022G>C GRCh37
NC_000006.10:g.106359715G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_942835.1:n.510+24910C>G
XR_001744274.1:n.438+24910C>G
XR_001744275.1:n.337+24910C>G
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