Canonical Allele Identifier: CA2499640167
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30911513G>T , CM000669.2:g.30911513G>T GRCh38
NC_000007.13:g.30951128G>T , CM000669.1:g.30951128G>T GRCh37
NC_000007.12:g.30917653G>T NCBI36
NG_007475.2:g.63120G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000509504.2:c.622-480G>T