Canonical Allele Identifier: CA168094791

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973824T>C , CM000669.2:g.141973824T>C GRCh38
NC_000007.13:g.141673624T>C , CM000669.1:g.141673624T>C GRCh37
NC_000007.12:g.141320093T>C NCBI36
NG_016141.1:g.4950A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27827T>C (MGAM) ENSP00000419372.1:n.-3+27827T>C
XM_011515783.1:c.*25-12572T>C (OR9A4) XP_011514085.1:n.*25-12572T>C