Canonical Allele Identifier: CA834335653

Linked Data

dbSNP Id: rs1187819204
MyVariant Identifiers: chr7:g.141927262T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141927262T>C , CM000669.2:g.141927262T>C GRCh38
NC_000007.13:g.141627062T>C , CM000669.1:g.141627062T>C GRCh37
NC_000007.12:g.141273531T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000465654.5:c.-179-18559T>C (MGAM) ENSP00000419372.1:n.-179-18559T>C
ENST00000497554.1:n.37-2515T>C (MGAM)
XM_011515783.1:c.*24+7418T>C (OR9A4) XP_011514085.1:n.*24+7418T>C