Canonical Allele Identifier: CA1083372880
Gene: ADAM19 HGNC NCBI

Linked Data

dbSNP Id: rs1756149009
gnomAD v3: 5-157518198-A-C
gnomAD v4: 5-157518198-A-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.157518198A>C , CM000667.2:g.157518198A>C GRCh38
NC_000005.9:g.156945206A>C , CM000667.1:g.156945206A>C GRCh37
NC_000005.8:g.156877784A>C NCBI36
NG_046960.1:g.62626T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000257527.9:c.666+625T>G MANE Select ENSP00000257527.5:n.666+625T>G
ENST00000257527.8:c.666+625T>G ENSP00000257527.4:n.666+625T>G
ENST00000517905.1:c.666+625T>G ENSP00000428654.1:n.666+625T>G
ENST00000517951.5:c.666+625T>G ENSP00000428376.1:n.666+625T>G
NM_033274.4:c.666+625T>G NP_150377.1:n.666+625T>G
XM_005266003.2:c.666+625T>G XP_005266060.1:n.666+625T>G
XM_011534680.1:c.-135-4693T>G XP_011532982.1:n.-135-4693T>G
XM_011534681.1:c.-145-4693T>G XP_011532983.1:n.-145-4693T>G
NM_033274.5:c.666+625T>G MANE Select NP_150377.1:n.666+625T>G
Search 100 bp 5'
Search 100 bp 3'