Canonical Allele Identifier: CA2223789361
Gene:

Linked Data

dbSNP Id: rs1964422838

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.55655449A>G , CM000678.2:g.55655449A>G GRCh38
NC_000016.9:g.55689361A>G , CM000678.1:g.55689361A>G GRCh37
NC_000016.8:g.54246862A>G NCBI36
NG_016969.1:g.4820A>G

Transcript Alleles

HGVS Amino-acid change
XR_933603.1:n.54+150T>C