Canonical Allele Identifier: CA150690485
Gene:

Linked Data

dbSNP Id: rs1030260949
gnomAD v3: 6-155812381-T-C
gnomAD v4: 6-155812381-T-C
MyVariant Identifiers: chr6:g.156133515T>C (hg19) chr6:g.155812381T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155812381T>C , CM000668.2:g.155812381T>C GRCh38
NC_000006.11:g.156133515T>C , CM000668.1:g.156133515T>C GRCh37
NC_000006.10:g.156175207T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+18962T>C
XR_943146.1:n.645-342A>G
XR_001744423.1:n.699-342A>G
XR_001744424.1:n.79+18962T>C
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