Canonical Allele Identifier: CA2773802988

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160668594T>C , CM000668.2:g.160668594T>C	GRCh38
NC_000006.11:g.161089626T>C , CM000668.1:g.161089626T>C	GRCh37
NC_000006.10:g.161009616T>C	NCBI36
NG_016147.1:g.2782A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452651.1:n.115-2221A>G