Canonical Allele Identifier: CA565162887
Gene:

Linked Data

dbSNP Id: rs1479348236
gnomAD v2: 6-1536095-A-C
gnomAD v3: 6-1535860-A-C
gnomAD v4: 6-1535860-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1535860A>C , CM000668.2:g.1535860A>C GRCh38
NC_000006.11:g.1536095A>C , CM000668.1:g.1536095A>C GRCh37
NC_000006.10:g.1481094A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_427861.2:n.234+16486T>G
XR_926380.1:n.218-2596A>C
XR_926381.1:n.1108-2596A>C
XR_926382.1:n.235-6681T>G
XR_926384.1:n.200-6681T>G
XR_001743921.1:n.235-6705T>G
XR_427861.3:n.234+16486T>G
XR_926381.2:n.1123-2596A>C