Canonical Allele Identifier: CA1038177550

Gene:

Linked Data

• dbSNP Id: rs370802064
• gnomAD v3: 2-155870546-G-C
• gnomAD v4: 2-155870546-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.155870546G>C , CM000664.2:g.155870546G>C	GRCh38
NC_000002.11:g.156727058G>C , CM000664.1:g.156727058G>C	GRCh37
NC_000002.10:g.156435304G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_923501.1:n.320-3359C>G
XR_001739749.1:n.331-29562C>G
XR_001739750.1:n.331-29562C>G
XR_001739751.1:n.331-29562C>G
XR_923501.2:n.331-3359C>G