Canonical Allele Identifier: CA130185899

Gene: ADAM19

Linked Data

• dbSNP Id: rs577028848
• gnomAD v2: 5-156945176-A-G
• gnomAD v3: 5-157518168-A-G
• gnomAD v4: 5-157518168-A-G
• MyVariant Identifiers: chr5:g.156945176A>G (hg19) ; chr5:g.157518168A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157518168A>G , CM000667.2:g.157518168A>G	GRCh38
NC_000005.9:g.156945176A>G , CM000667.1:g.156945176A>G	GRCh37
NC_000005.8:g.156877754A>G	NCBI36
NG_046960.1:g.62656T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000257527.9:c.666+655T>C MANE Select	ENSP00000257527.5:n.666+655T>C
ENST00000257527.8:c.666+655T>C	ENSP00000257527.4:n.666+655T>C
ENST00000517905.1:c.666+655T>C	ENSP00000428654.1:n.666+655T>C
ENST00000517951.5:c.666+655T>C	ENSP00000428376.1:n.666+655T>C
NM_033274.4:c.666+655T>C	NP_150377.1:n.666+655T>C
XM_005266003.2:c.666+655T>C	XP_005266060.1:n.666+655T>C
XM_011534680.1:c.-135-4663T>C	XP_011532982.1:n.-135-4663T>C
XM_011534681.1:c.-145-4663T>C	XP_011532983.1:n.-145-4663T>C
NM_033274.5:c.666+655T>C MANE Select	NP_150377.1:n.666+655T>C