Canonical Allele Identifier: CA563691814
Gene: ADAM19 HGNC NCBI

Linked Data

dbSNP Id: rs1447428695
gnomAD v2: 5-156970186-A-C
gnomAD v3: 5-157543178-A-C
gnomAD v4: 5-157543178-A-C
MyVariant Identifiers: chr5:g.156970186A>C (hg19) chr5:g.157543178A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.157543178A>C , CM000667.2:g.157543178A>C GRCh38
NC_000005.9:g.156970186A>C , CM000667.1:g.156970186A>C GRCh37
NC_000005.8:g.156902764A>C NCBI36
NG_046960.1:g.37646T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000257527.9:c.252-5187T>G MANE Select ENSP00000257527.5:n.252-5187T>G
ENST00000257527.8:c.252-5187T>G ENSP00000257527.4:n.252-5187T>G
ENST00000517905.1:c.252-5187T>G ENSP00000428654.1:n.252-5187T>G
ENST00000517951.5:c.252-5187T>G ENSP00000428376.1:n.252-5187T>G
NM_033274.4:c.252-5187T>G NP_150377.1:n.252-5187T>G
XM_005266003.2:c.252-5187T>G XP_005266060.1:n.252-5187T>G
NM_033274.5:c.252-5187T>G MANE Select NP_150377.1:n.252-5187T>G
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