Canonical Allele Identifier: CA150690531
Gene:

Linked Data

dbSNP Id: rs186062211
gnomAD v2: 6-156133852-A-G
gnomAD v3: 6-155812718-A-G
gnomAD v4: 6-155812718-A-G
MyVariant Identifiers: chr6:g.156133852A>G (hg19) chr6:g.155812718A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155812718A>G , CM000668.2:g.155812718A>G GRCh38
NC_000006.11:g.156133852A>G , CM000668.1:g.156133852A>G GRCh37
NC_000006.10:g.156175544A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+19299A>G
XR_943146.1:n.645-679T>C
XR_001744423.1:n.699-679T>C
XR_001744424.1:n.79+19299A>G
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