Canonical Allele Identifier: CA1677169919
Gene:

Linked Data

dbSNP Id: rs372391993
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160668541T>G , CM000668.2:g.160668541T>G GRCh38
NC_000006.11:g.161089573T>G , CM000668.1:g.161089573T>G GRCh37
NC_000006.10:g.161009563T>G NCBI36
NG_016147.1:g.2835A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000452651.1:n.115-2168A>C
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