Canonical Allele Identifier: CA447449742
Gene: ADAM19 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.156995914A>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.157568906A>C , CM000667.2:g.157568906A>C GRCh38
NC_000005.9:g.156995914A>C , CM000667.1:g.156995914A>C GRCh37
NC_000005.8:g.156928492A>C NCBI36
NG_046960.1:g.11918T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000257527.9:c.180+1989T>G MANE Select ENSP00000257527.5:n.180+1989T>G
ENST00000257527.8:c.180+1989T>G ENSP00000257527.4:n.180+1989T>G
ENST00000517905.1:c.180+1989T>G ENSP00000428654.1:n.180+1989T>G
ENST00000517951.5:c.180+1989T>G ENSP00000428376.1:n.180+1989T>G
NM_033274.4:c.180+1989T>G NP_150377.1:n.180+1989T>G
XM_005266003.2:c.180+1989T>G XP_005266060.1:n.180+1989T>G
NM_033274.5:c.180+1989T>G MANE Select NP_150377.1:n.180+1989T>G
Search 100 bp 5'
Search 100 bp 3'