Canonical Allele Identifier: CA150162827

Gene:

Linked Data

• dbSNP Id: rs1010022863
• gnomAD v2: 6-151954658-C-T
• gnomAD v3: 6-151633523-C-T
• gnomAD v4: 6-151633523-C-T
• MyVariant Identifiers: chr6:g.151954658C>T (hg19) ; chr6:g.151633523C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151633523C>T , CM000668.2:g.151633523C>T	GRCh38
NC_000006.11:g.151954658C>T , CM000668.1:g.151954658C>T	GRCh37
NC_000006.10:g.151996351C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943115.1:n.2496+3541C>T