Canonical Allele Identifier: CA820839117

Gene:

Linked Data

• dbSNP Id: rs1265087616
• MyVariant Identifiers: chr6:g.151954545C>T (hg19) ; chr6:g.151633410C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151633410C>T , CM000668.2:g.151633410C>T	GRCh38
NC_000006.11:g.151954545C>T , CM000668.1:g.151954545C>T	GRCh37
NC_000006.10:g.151996238C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943115.1:n.2496+3428C>T