Canonical Allele Identifier: CA151622545
Gene:

Linked Data

dbSNP Id: rs551627560
gnomAD v3: 6-163765624-A-G
gnomAD v4: 6-163765624-A-G
MyVariant Identifiers: chr6:g.164186656A>G (hg19) chr6:g.163765624A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.163765624A>G , CM000668.2:g.163765624A>G GRCh38
NC_000006.11:g.164186656A>G , CM000668.1:g.164186656A>G GRCh37
NC_000006.10:g.164106646A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001744452.1:n.410+6195A>G
XR_001744454.1:n.369+6236A>G
XR_001744455.1:n.346+6259A>G
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