Canonical Allele Identifier: CA834335659

Linked Data

dbSNP Id: rs1291503708
MyVariant Identifiers: chr7:g.141927291C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141927291C>T , CM000669.2:g.141927291C>T GRCh38
NC_000007.13:g.141627091C>T , CM000669.1:g.141627091C>T GRCh37
NC_000007.12:g.141273560C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000465654.5:c.-179-18530C>T (MGAM) ENSP00000419372.1:n.-179-18530C>T
ENST00000497554.1:n.37-2486C>T (MGAM)
XM_011515783.1:c.*24+7447C>T (OR9A4) XP_011514085.1:n.*24+7447C>T