Canonical Allele Identifier: CA150690500
Gene:

Linked Data

dbSNP Id: rs1049848452
gnomAD v3: 6-155812463-A-G
gnomAD v4: 6-155812463-A-G
MyVariant Identifiers: chr6:g.156133597A>G (hg19) chr6:g.155812463A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155812463A>G , CM000668.2:g.155812463A>G GRCh38
NC_000006.11:g.156133597A>G , CM000668.1:g.156133597A>G GRCh37
NC_000006.10:g.156175289A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+19044A>G
XR_943146.1:n.645-424T>C
XR_001744423.1:n.699-424T>C
XR_001744424.1:n.79+19044A>G
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