Canonical Allele Identifier: CA830043412
Gene:

Linked Data

dbSNP Id: rs1470443470
MyVariant Identifiers: chr6:g.95967334A>T (hg19) chr6:g.95519458A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.95519458A>T , CM000668.2:g.95519458A>T GRCh38
NC_000006.11:g.95967334A>T , CM000668.1:g.95967334A>T GRCh37
NC_000006.10:g.96074055A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_942795.1:n.108T>A
Search 100 bp 5'
Search 100 bp 3'