Canonical Allele Identifier: CA821666546

Gene:

Linked Data

• dbSNP Id: rs1376658972
• gnomAD v3: 6-160668481-A-G
• gnomAD v4: 6-160668481-A-G
• MyVariant Identifiers: chr6:g.161089513A>G (hg19) ; chr6:g.160668481A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160668481A>G , CM000668.2:g.160668481A>G	GRCh38
NC_000006.11:g.161089513A>G , CM000668.1:g.161089513A>G	GRCh37
NC_000006.10:g.161009503A>G	NCBI36
NG_016147.1:g.2895T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452651.1:n.115-2108T>C