Canonical Allele Identifier: CA16284810
Gene:
dbSNP:
10499298
gnomAD v2:
6:156134070 C / T
gnomAD v3:
6:155812936 C / T
gnomAD v4:
chr6-155812936-C-T
Joint Max Group AF 0.13460128 (AMR)
Genomes Max Group AF 0.13460128 (AMR)
MyVariant.info:
GRCh38 chr6:g.155812936C>T
GRCh37 chr6:g.156134070C>T
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155812936C>T , CM000668.2:g.155812936C>T GRCh38
NC_000006.11:g.156134070C>T , CM000668.1:g.156134070C>T GRCh37
NC_000006.10:g.156175762C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+19517C>T
XR_943146.1:n.645-897G>A
XR_001744423.1:n.699-897G>A
XR_001744424.1:n.79+19517C>T
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