Canonical Allele Identifier: CA820925258
Gene:

Linked Data

dbSNP Id: rs1489649111
MyVariant Identifiers: chr6:g.1535808A>G (hg19) chr6:g.1535573A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1535573A>G , CM000668.2:g.1535573A>G GRCh38
NC_000006.11:g.1535808A>G , CM000668.1:g.1535808A>G GRCh37
NC_000006.10:g.1480807A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_427861.2:n.234+16773T>C
XR_926380.1:n.218-2883A>G
XR_926381.1:n.1108-2883A>G
XR_926382.1:n.235-6394T>C
XR_926384.1:n.200-6394T>C
XR_001743921.1:n.235-6418T>C
XR_427861.3:n.234+16773T>C
XR_926381.2:n.1123-2883A>G
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