Canonical Allele Identifier: CA12228642
Gene:

Linked Data

dbSNP Id: rs198846

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26107235A>G , CM000668.2:g.26107235A>G GRCh38
NC_000006.11:g.26107463A>G , CM000668.1:g.26107463A>G GRCh37
NC_000006.10:g.26215442A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000629531.1:n.132+16538T>C ENSP00000486472.1:p.=