Canonical Allele Identifier: CA571557131
Gene:

Linked Data

dbSNP Id: rs1156717586
gnomAD v2: 6-161089762-C-G
gnomAD v3: 6-160668730-C-G
gnomAD v4: 6-160668730-C-G
MyVariant Identifiers: chr6:g.161089762C>G (hg19) chr6:g.160668730C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160668730C>G , CM000668.2:g.160668730C>G GRCh38
NC_000006.11:g.161089762C>G , CM000668.1:g.161089762C>G GRCh37
NC_000006.10:g.161009752C>G NCBI36
NG_016147.1:g.2646G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000452651.1:n.115-2357G>C
Search 100 bp 5'
Search 100 bp 3'