Canonical Allele Identifier: CA133613612
Gene:

Linked Data

dbSNP Id: rs931779975
gnomAD v3: 6-1535932-G-A
gnomAD v4: 6-1535932-G-A
MyVariant Identifiers: chr6:g.1536167G>A (hg19) chr6:g.1535932G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1535932G>A , CM000668.2:g.1535932G>A GRCh38
NC_000006.11:g.1536167G>A , CM000668.1:g.1536167G>A GRCh37
NC_000006.10:g.1481166G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_427861.2:n.234+16414C>T
XR_926380.1:n.218-2524G>A
XR_926381.1:n.1108-2524G>A
XR_926382.1:n.235-6753C>T
XR_926384.1:n.200-6753C>T
XR_001743921.1:n.235-6777C>T
XR_427861.3:n.234+16414C>T
XR_926381.2:n.1123-2524G>A
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