Canonical Allele Identifier: CA742353491

Gene:

Linked Data

• dbSNP Id: rs1463930839
• gnomAD v4: 20-2470860-C-T
• MyVariant Identifiers: chr20:g.2451506C>T (hg19) ; chr20:g.2470860C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.2470860C>T , CM000682.2:g.2470860C>T	GRCh38
NC_000020.10:g.2451506C>T , CM000682.1:g.2451506C>T	GRCh37
NC_000020.9:g.2399506C>T	NCBI36
NG_042057.1:g.4994G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461548.1:c.305-3102G>A	ENSP00000456213.1:n.305-3102G>A