Canonical Allele Identifier: CA150690483
Gene:

Linked Data

dbSNP Id: rs1019021627
gnomAD v2: 6-156133489-G-A
gnomAD v3: 6-155812355-G-A
gnomAD v4: 6-155812355-G-A
MyVariant Identifiers: chr6:g.156133489G>A (hg19) chr6:g.155812355G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155812355G>A , CM000668.2:g.155812355G>A GRCh38
NC_000006.11:g.156133489G>A , CM000668.1:g.156133489G>A GRCh37
NC_000006.10:g.156175181G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+18936G>A
XR_943146.1:n.645-316C>T
XR_001744423.1:n.699-316C>T
XR_001744424.1:n.79+18936G>A
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