Canonical Allele Identifier: CA821223720
Gene:

Linked Data

dbSNP Id: rs1343203369
gnomAD v3: 6-155812665-A-C
gnomAD v4: 6-155812665-A-C
MyVariant Identifiers: chr6:g.156133799A>C (hg19) chr6:g.155812665A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155812665A>C , CM000668.2:g.155812665A>C GRCh38
NC_000006.11:g.156133799A>C , CM000668.1:g.156133799A>C GRCh37
NC_000006.10:g.156175491A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+19246A>C
XR_943146.1:n.645-626T>G
XR_001744423.1:n.699-626T>G
XR_001744424.1:n.79+19246A>C
Search 100 bp 5'
Search 100 bp 3'