Canonical Allele Identifier: CA150691057
Gene:

Linked Data

dbSNP Id: rs191885460
gnomAD v2: 6-156138826-A-C
gnomAD v3: 6-155817692-A-C
gnomAD v4: 6-155817692-A-C
MyVariant Identifiers: chr6:g.156138826A>C (hg19) chr6:g.155817692A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155817692A>C , CM000668.2:g.155817692A>C GRCh38
NC_000006.11:g.156138826A>C , CM000668.1:g.156138826A>C GRCh37
NC_000006.10:g.156180518A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943142.1:n.79+24273A>C
XR_943146.1:n.552-3022T>G
XR_001744423.1:n.606-3022T>G
XR_001744424.1:n.79+24273A>C
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