Canonical Allele Identifier: CA150690494
Gene:

Linked Data

dbSNP Id: rs978938960
gnomAD v2: 6-156133570-T-C
gnomAD v3: 6-155812436-T-C
gnomAD v4: 6-155812436-T-C
MyVariant Identifiers: chr6:g.156133570T>C (hg19) chr6:g.155812436T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155812436T>C , CM000668.2:g.155812436T>C GRCh38
NC_000006.11:g.156133570T>C , CM000668.1:g.156133570T>C GRCh37
NC_000006.10:g.156175262T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+19017T>C
XR_943146.1:n.645-397A>G
XR_001744423.1:n.699-397A>G
XR_001744424.1:n.79+19017T>C
Search 100 bp 5'
Search 100 bp 3'