Canonical Allele Identifier: CA1092237086
Gene:

Linked Data

dbSNP Id: rs777891534
gnomAD v3: 6-98048101-G-C
gnomAD v4: 6-98048101-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98048101G>C , CM000668.2:g.98048101G>C GRCh38
NC_000006.11:g.98495977G>C , CM000668.1:g.98495977G>C GRCh37
NC_000006.10:g.98602698G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245563.2:n.372-51085G>C
XR_942809.1:n.372-51085G>C