Canonical Allele Identifier: CA150159395

Gene:

Linked Data

• dbSNP Id: rs893147286
• gnomAD v2: 6-151948316-C-T
• gnomAD v3: 6-151627181-C-T
• gnomAD v4: 6-151627181-C-T
• MyVariant Identifiers: chr6:g.151948316C>T (hg19) ; chr6:g.151627181C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151627181C>T , CM000668.2:g.151627181C>T	GRCh38
NC_000006.11:g.151948316C>T , CM000668.1:g.151948316C>T	GRCh37
NC_000006.10:g.151990009C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_943113.1:n.607C>T
XR_943115.1:n.607C>T