Canonical Allele Identifier: CA820925369
Gene:

Linked Data

dbSNP Id: rs1254247042
MyVariant Identifiers: chr6:g.1536114G>A (hg19) chr6:g.1535879G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1535879G>A , CM000668.2:g.1535879G>A GRCh38
NC_000006.11:g.1536114G>A , CM000668.1:g.1536114G>A GRCh37
NC_000006.10:g.1481113G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_427861.2:n.234+16467C>T
XR_926380.1:n.218-2577G>A
XR_926381.1:n.1108-2577G>A
XR_926382.1:n.235-6700C>T
XR_926384.1:n.200-6700C>T
XR_001743921.1:n.235-6724C>T
XR_427861.3:n.234+16467C>T
XR_926381.2:n.1123-2577G>A
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