Canonical Allele Identifier: CA133346672
Gene:

Linked Data

dbSNP Id: rs151198311
gnomAD v2: 6-465983-T-C
gnomAD v3: 6-465983-T-C
gnomAD v4: 6-465983-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.465983T>C , CM000668.2:g.465983T>C GRCh38
NC_000006.11:g.465983T>C , CM000668.1:g.465983T>C GRCh37
NC_000006.10:g.410983T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_926364.1:n.2714+12258T>C
XR_926365.1:n.2548+12258T>C
XR_001743914.1:n.482-9225T>C