Canonical Allele Identifier: CA134173710
Gene:

Linked Data

dbSNP Id: rs937899059
gnomAD v3: 6-11943528-T-C
gnomAD v4: 6-11943528-T-C
MyVariant Identifiers: chr6:g.11943761T>C (hg19) chr6:g.11943528T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.11943528T>C , CM000668.2:g.11943528T>C GRCh38
NC_000006.11:g.11943761T>C , CM000668.1:g.11943761T>C GRCh37
NC_000006.10:g.12051747T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001743976.1:n.348-8007T>C
Search 100 bp 5'
Search 100 bp 3'