Canonical Allele Identifier: CA571581177
Gene:

Linked Data

dbSNP Id: rs1187383065
gnomAD v2: 6-156133875-C-A
gnomAD v3: 6-155812741-C-A
gnomAD v4: 6-155812741-C-A
MyVariant Identifiers: chr6:g.156133875C>A (hg19) chr6:g.155812741C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155812741C>A , CM000668.2:g.155812741C>A GRCh38
NC_000006.11:g.156133875C>A , CM000668.1:g.156133875C>A GRCh37
NC_000006.10:g.156175567C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+19322C>A
XR_943146.1:n.645-702G>T
XR_001744423.1:n.699-702G>T
XR_001744424.1:n.79+19322C>A
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