Canonical Allele Identifier: CA2769720758
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.466003G>C , CM000668.2:g.466003G>C GRCh38
NC_000006.11:g.466003G>C , CM000668.1:g.466003G>C GRCh37
NC_000006.10:g.411003G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_926364.1:n.2714+12278G>C
XR_926365.1:n.2548+12278G>C
XR_001743914.1:n.482-9205G>C