Canonical Allele Identifier: CA837538659

Gene:

Linked Data

• dbSNP Id: rs968872833
• MyVariant Identifiers: chr7:g.30937041G>T (hg19) ; chr7:g.30897426G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30897426G>T , CM000669.2:g.30897426G>T	GRCh38
NC_000007.13:g.30937041G>T , CM000669.1:g.30937041G>T	GRCh37
NC_000007.12:g.30903566G>T	NCBI36
NG_007475.2:g.49033G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509504.2:c.621+14433G>T