Canonical Allele Identifier: CA571813965
Gene:

Linked Data

dbSNP Id: rs1238407303
gnomAD v2: 6-164186615-C-A
gnomAD v3: 6-163765583-C-A
gnomAD v4: 6-163765583-C-A
MyVariant Identifiers: chr6:g.164186615C>A (hg19) chr6:g.163765583C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.163765583C>A , CM000668.2:g.163765583C>A GRCh38
NC_000006.11:g.164186615C>A , CM000668.1:g.164186615C>A GRCh37
NC_000006.10:g.164106605C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001744452.1:n.410+6154C>A
XR_001744454.1:n.369+6195C>A
XR_001744455.1:n.346+6218C>A
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