Canonical Allele Identifier: CA281436463
Gene:

Linked Data

dbSNP Id: rs1045495169
MyVariant Identifiers: chr16:g.55655466G>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.55655466G>T , CM000678.2:g.55655466G>T GRCh38
NC_000016.9:g.55689378G>T , CM000678.1:g.55689378G>T GRCh37
NC_000016.8:g.54246879G>T NCBI36
NG_016969.1:g.4837G>T

Transcript Alleles

HGVS Amino-acid change
XR_933603.1:n.54+133C>A