Canonical Allele Identifier: CA149263612
Gene:

Linked Data

dbSNP Id: rs11155133
gnomAD v2: 6-141169825-A-G
gnomAD v3: 6-140848688-A-G
gnomAD v4: 6-140848688-A-G
MyVariant Identifiers: chr6:g.141169825A>G (hg19) chr6:g.140848688A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.140848688A>G , CM000668.2:g.140848688A>G GRCh38
NC_000006.11:g.141169825A>G , CM000668.1:g.141169825A>G GRCh37
NC_000006.10:g.141211518A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_428030.2:n.327-2384T>C
XR_943075.1:n.315-2384T>C
XR_943076.1:n.246-2384T>C
XR_001744390.1:n.235-32458T>C
XR_428030.4:n.341-2384T>C
XR_943075.3:n.329-2384T>C
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