Canonical Allele Identifier: CA571557082

Gene:

Linked Data

• dbSNP Id: rs1244094941
• gnomAD v2: 6-161089739-G-T
• gnomAD v3: 6-160668707-G-T
• gnomAD v4: 6-160668707-G-T
• MyVariant Identifiers: chr6:g.161089739G>T (hg19) ; chr6:g.160668707G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160668707G>T , CM000668.2:g.160668707G>T	GRCh38
NC_000006.11:g.161089739G>T , CM000668.1:g.161089739G>T	GRCh37
NC_000006.10:g.161009729G>T	NCBI36
NG_016147.1:g.2669C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000452651.1:n.115-2334C>A