Canonical Allele Identifier: CA834339469

Linked Data

dbSNP Id: rs1163158928
MyVariant Identifiers: chr7:g.141973858A>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973858A>C , CM000669.2:g.141973858A>C GRCh38
NC_000007.13:g.141673658A>C , CM000669.1:g.141673658A>C GRCh37
NC_000007.12:g.141320127A>C NCBI36
NG_016141.1:g.4916T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27861A>C (MGAM) ENSP00000419372.1:n.-3+27861A>C
XM_011515783.1:c.*25-12538A>C (OR9A4) XP_011514085.1:n.*25-12538A>C