Canonical Allele Identifier: CA2769749872
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1535815C>T , CM000668.2:g.1535815C>T GRCh38
NC_000006.11:g.1536050C>T , CM000668.1:g.1536050C>T GRCh37
NC_000006.10:g.1481049C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_427861.2:n.234+16531G>A
XR_926380.1:n.218-2641C>T
XR_926381.1:n.1108-2641C>T
XR_926382.1:n.235-6636G>A
XR_926384.1:n.200-6636G>A
XR_001743921.1:n.235-6660G>A
XR_427861.3:n.234+16531G>A
XR_926381.2:n.1123-2641C>T