Canonical Allele Identifier: CA1605794999
Gene:

Linked Data

dbSNP Id: rs1761315470
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1535588C>T , CM000668.2:g.1535588C>T GRCh38
NC_000006.11:g.1535823C>T , CM000668.1:g.1535823C>T GRCh37
NC_000006.10:g.1480822C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_427861.2:n.234+16758G>A
XR_926380.1:n.218-2868C>T
XR_926381.1:n.1108-2868C>T
XR_926382.1:n.235-6409G>A
XR_926384.1:n.200-6409G>A
XR_001743921.1:n.235-6433G>A
XR_427861.3:n.234+16758G>A
XR_926381.2:n.1123-2868C>T
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