Canonical Allele Identifier: CA825142469
Gene:

Linked Data

dbSNP Id: rs1204467126
gnomAD v3: 6-465856-T-C
gnomAD v4: 6-465856-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.465856T>C , CM000668.2:g.465856T>C GRCh38
NC_000006.11:g.465856T>C , CM000668.1:g.465856T>C GRCh37
NC_000006.10:g.410856T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926364.1:n.2714+12131T>C
XR_926365.1:n.2548+12131T>C
XR_001743914.1:n.482-9352T>C