Canonical Allele Identifier: CA834339495

Linked Data

dbSNP Id: rs1164692469
MyVariant Identifiers: chr7:g.141973983A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973983A>G , CM000669.2:g.141973983A>G GRCh38
NC_000007.13:g.141673783A>G , CM000669.1:g.141673783A>G GRCh37
NC_000007.12:g.141320252A>G NCBI36
NG_016141.1:g.4791T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27986A>G (MGAM) ENSP00000419372.1:n.-3+27986A>G
XM_011515783.1:c.*25-12413A>G (OR9A4) XP_011514085.1:n.*25-12413A>G