Canonical Allele Identifier: CA230605984

Gene:

Linked Data

• dbSNP Id: rs921051058
• MyVariant Identifiers: chr11:g.128870888A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128870888A>T , CM000673.2:g.128870888A>T	GRCh38
NC_000011.9:g.128740783A>T , CM000673.1:g.128740783A>T	GRCh37
NC_000011.8:g.128245993A>T	NCBI36
NG_009379.1:g.1486T>A

Transcript Alleles

HGVS	Amino-acid Change
XR_948172.1:n.6023T>A
XR_948173.1:n.5712T>A