Canonical Allele Identifier: CA150690487
Gene:

Linked Data

dbSNP Id: rs988637789
gnomAD v2: 6-156133549-G-C
gnomAD v3: 6-155812415-G-C
gnomAD v4: 6-155812415-G-C
MyVariant Identifiers: chr6:g.156133549G>C (hg19) chr6:g.155812415G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155812415G>C , CM000668.2:g.155812415G>C GRCh38
NC_000006.11:g.156133549G>C , CM000668.1:g.156133549G>C GRCh37
NC_000006.10:g.156175241G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+18996G>C
XR_943146.1:n.645-376C>G
XR_001744423.1:n.699-376C>G
XR_001744424.1:n.79+18996G>C
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