Canonical Allele Identifier: CA1672979169

Gene:

Linked Data

• dbSNP Id: rs1582811589
• gnomAD v3: 6-151633630-T-C
• gnomAD v4: 6-151633630-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151633630T>C , CM000668.2:g.151633630T>C	GRCh38
NC_000006.11:g.151954765T>C , CM000668.1:g.151954765T>C	GRCh37
NC_000006.10:g.151996458T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943115.1:n.2496+3648T>C