Canonical Allele Identifier: CA150691058
Gene:

Linked Data

dbSNP Id: rs1043932705
gnomAD v3: 6-155817704-C-T
gnomAD v4: 6-155817704-C-T
MyVariant Identifiers: chr6:g.156138838C>T (hg19) chr6:g.155817704C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155817704C>T , CM000668.2:g.155817704C>T GRCh38
NC_000006.11:g.156138838C>T , CM000668.1:g.156138838C>T GRCh37
NC_000006.10:g.156180530C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+24285C>T
XR_943146.1:n.552-3034G>A
XR_001744423.1:n.606-3034G>A
XR_001744424.1:n.79+24285C>T
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