Canonical Allele Identifier: CA821666586

Gene:

Linked Data

• dbSNP Id: rs1395595372
• gnomAD v3: 6-160668546-G-T
• gnomAD v4: 6-160668546-G-T
• MyVariant Identifiers: chr6:g.161089578G>T (hg19) ; chr6:g.160668546G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160668546G>T , CM000668.2:g.160668546G>T	GRCh38
NC_000006.11:g.161089578G>T , CM000668.1:g.161089578G>T	GRCh37
NC_000006.10:g.161009568G>T	NCBI36
NG_016147.1:g.2830C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452651.1:n.115-2173C>A