Canonical Allele Identifier: CA2769114798
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159333222T>G , CM000667.2:g.159333222T>G GRCh38
NC_000005.9:g.158760230T>G , CM000667.1:g.158760230T>G GRCh37
NC_000005.8:g.158692808T>G NCBI36
NG_009618.1:g.2252A>C , LRG_71:g.2252A>C

Transcript Alleles

HGVS Amino-acid Change
NR_037889.1:n.745+219T>G